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Specialist Nutrition Support Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Radiographer
Job summary We have an exciting opportunity for an experienced and driven registered nurse to join our Specialist Nutrition Support Nurse team (band 6, 26.
10 day(s) ago
Specialist Nutrition Support Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Radiographer
Job summary We have an exciting opportunity for an experienced and driven registered nurse to join our Specialist Nutrition Support Nurse team (band 6, 26.
10 day(s) ago
Clinical Nurse Specialist
The Christie NHS FT
Greater Manchester, North West England
GBP 49,387 - 56,515 per year
Haematologist
Job summary An exciting opportunity has arisen for an experienced and motivated nurse to join the Clinical Apheresis Unit (CAU) within the Haematology and Tran…
10 day(s) ago
Clinical Nurse Specialist
The Christie NHS FT
Greater Manchester, North West England
GBP 49,387 - 56,515 per year
Haematologist
Job summary An exciting opportunity has arisen for an experienced and motivated nurse to join the Clinical Apheresis Unit (CAU) within the Haematology and Tran…
10 day(s) ago
Clinical Trials Coordinator
The Christie NHS FT
Greater Manchester, North West England
GBP 25,760 - 31,157 per year
Gynaecologist
Job summary This post is offered at 37.5 hours per week but we are happy to access flexible working or part time working requests. We are looking to appoint a…
10 day(s) ago
Clinical Trials Coordinator
The Christie NHS FT
Greater Manchester, North West England
GBP 25,760 - 31,157 per year
Gynaecologist
Job summary This post is offered at 37.5 hours per week but we are happy to access flexible working or part time working requests. We are looking to appoint a…
10 day(s) ago
Staff Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary The Integrated Procedures Unit (IPU) has an exciting opportunity for a highly motivated, organised and competent Staff Nurse to join our core nursi…
10 day(s) ago
Staff Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary The Integrated Procedures Unit (IPU) has an exciting opportunity for a highly motivated, organised and competent Staff Nurse to join our core nursi…
10 day(s) ago
Support Secretary
The Christie NHS FT
Greater Manchester, North West England
GBP 25,760 - 27,476 per year
Radiographer
Job summary An exciting opportunity has arisen for an enthusiastic individual to become part of the Palliative and Supportive Care Teams, rotation will be requ…
25 day(s) ago
Support Secretary
The Christie NHS FT
Greater Manchester, North West England
GBP 25,760 - 27,476 per year
Radiographer
Job summary An exciting opportunity has arisen for an enthusiastic individual to become part of the Palliative and Supportive Care Teams, rotation will be requ…
25 day(s) ago
ACP Teenage and Young Adult (Haematology & Oncology)
The Christie NHS FT
Greater Manchester, North West England
GBP 57,528 - 64,750 per year
Haematologist
Job summary An incredible opportunity has arisen to become part of our specialist Haematology and Transplant team at The Christie, delivering cutting-edge care…
25 day(s) ago
ACP Teenage and Young Adult (Haematology & Oncology)
The Christie NHS FT
Greater Manchester, North West England
GBP 57,528 - 64,750 per year
Haematologist
Job summary An incredible opportunity has arisen to become part of our specialist Haematology and Transplant team at The Christie, delivering cutting-edge care…
25 day(s) ago
Senior Healthcare Assistant
The Christie NHS FT
Greater Manchester, North West England
GBP 25,760 - 27,476 per year
Radiographer
Job summary Join our collaborative SACT Outreach and Bloods Closer to Home team, supporting satellite sites across Greater Manchester and Cheshire.
25 day(s) ago
Senior Healthcare Assistant
The Christie NHS FT
Greater Manchester, North West England
GBP 25,760 - 27,476 per year
Radiographer
Job summary Join our collaborative SACT Outreach and Bloods Closer to Home team, supporting satellite sites across Greater Manchester and Cheshire.
25 day(s) ago
Specialist Clinical Pharmacist - Clinical Haematology
The Christie NHS FT
Inner London, Greater London
GBP 57,528 - 64,750 per year
GP/General Practitioner
Job summary We are one of the largest oncology Trusts in the UK with an international reputation for clinical excellence, research and development.
1 month(s) ago
Specialist Clinical Pharmacist - Clinical Haematology
The Christie NHS FT
Inner London, Greater London
GBP 57,528 - 64,750 per year
GP/General Practitioner
Job summary We are one of the largest oncology Trusts in the UK with an international reputation for clinical excellence, research and development.
1 month(s) ago
Staff Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Oncologist
Job summary Acute Assessment Unit Band 5 Registered Nurse 34.
1 month(s) ago
Staff Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Oncologist
Job summary Acute Assessment Unit Band 5 Registered Nurse 34.
1 month(s) ago
Senior Domestic Supervisor
The Christie NHS FT
Greater Manchester, North West England
GBP 28,392 - 31,157 per year
Radiographer
Job summary We are seeking a motivated and aspiring Senior Supervisor to join the supervisory team within the Estate and Facilities Division, Site Services Dir…
1 month(s) ago
Senior Domestic Supervisor
The Christie NHS FT
Greater Manchester, North West England
GBP 28,392 - 31,157 per year
Radiographer
Job summary We are seeking a motivated and aspiring Senior Supervisor to join the supervisory team within the Estate and Facilities Division, Site Services Dir…
1 month(s) ago
Clinical Trials Co-ordinator
The Christie NHS FT
Greater Manchester, North West England
GBP 28,392 - 31,157 per year
Radiographer
Job summary The main purpose of the role is to support the Experimental Cancer Medicine Team with all aspects of clinical trials administration, according to G…
1 month(s) ago
Clinical Trials Co-ordinator
The Christie NHS FT
Greater Manchester, North West England
GBP 28,392 - 31,157 per year
Radiographer
Job summary The main purpose of the role is to support the Experimental Cancer Medicine Team with all aspects of clinical trials administration, according to G…
1 month(s) ago
Assistant Clinical Governance Manager
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
General Surgeon
Job summary Are you passionate about Patient Safety and Experience and wish to support staff to improve care?
1 month(s) ago
Assistant Clinical Governance Manager
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
General Surgeon
Job summary Are you passionate about Patient Safety and Experience and wish to support staff to improve care?
1 month(s) ago
Clinical Research Practitioner
The Christie NHS FT
Greater Manchester, North West England
GBP 28,392 - 31,157 per year
Gynaecologist
Job summary Please note that these posts are permanent contracts at 37.
1 month(s) ago
Clinical Research Practitioner
The Christie NHS FT
Greater Manchester, North West England
GBP 28,392 - 31,157 per year
Gynaecologist
Job summary Please note that these posts are permanent contracts at 37.
1 month(s) ago
Senior Radiographer
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Radiographer
Job summary We are looking for hardworking team players to join us in the friendly Radiotherapy treatment delivery teams at all The Christie sites-Withington,…
1 month(s) ago
Senior Radiographer
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Radiographer
Job summary We are looking for hardworking team players to join us in the friendly Radiotherapy treatment delivery teams at all The Christie sites-Withington,…
1 month(s) ago
PA/Medical Secretary
The Christie NHS FT
Greater Manchester, North West England
GBP 28,392 - 31,157 per year
Gynaecologist
Job summary An exciting opportunity has arisen for a well-motivated individual to join us as a PA/Medical Secretary in the Oncology Department within Networked…
1 month(s) ago
PA/Medical Secretary
The Christie NHS FT
Greater Manchester, North West England
GBP 28,392 - 31,157 per year
Gynaecologist
Job summary An exciting opportunity has arisen for a well-motivated individual to join us as a PA/Medical Secretary in the Oncology Department within Networked…
1 month(s) ago
Clinical Research Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Gynaecologist
Job summary We are looking for a highly motivated nurse to join the Experimental Cancer Medicine Team (ECMT) at The Christie NHS Foundation Trust.
1 month(s) ago
Clinical Research Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Gynaecologist
Job summary We are looking for a highly motivated nurse to join the Experimental Cancer Medicine Team (ECMT) at The Christie NHS Foundation Trust.
1 month(s) ago
Research Quality Assurance Manager
The Christie NHS FT
Greater Manchester, North West England
GBP 49,387 - 56,515 per year
Radiographer
Job summary An exciting opportunity has arisen for an experienced research professional to join The Christie Research and Innovation Division as a Research Qua…
1 month(s) ago
Research Quality Assurance Manager
The Christie NHS FT
Greater Manchester, North West England
GBP 49,387 - 56,515 per year
Radiographer
Job summary An exciting opportunity has arisen for an experienced research professional to join The Christie Research and Innovation Division as a Research Qua…
1 month(s) ago
Clinical Research Fellow in Cancer Imaging
The Christie NHS FT
Greater Manchester, North West England
GBP 55,355 - 76,582 per year
Interventional Radiologist
Job summary We are seeking an ambitious, innovative individual with a specific interest in cancer imaging and/or colorectal cancers / MR imaging to work on the…
1 month(s) ago
Clinical Research Fellow in Cancer Imaging
The Christie NHS FT
Greater Manchester, North West England
GBP 55,355 - 76,582 per year
Interventional Radiologist
Job summary We are seeking an ambitious, innovative individual with a specific interest in cancer imaging and/or colorectal cancers / MR imaging to work on the…
1 month(s) ago
Consultant Medical Oncology - Colorectal Oncology
The Christie NHS FT
Greater Manchester, North West England
GBP 113,565 - 150,569 per year
Gynaecologist
Job summary This post is for 8 Programmed Activities (PAs) per week to work within the Medical Oncology Colorectal Disease Group mainly based at The Christie s…
1 month(s) ago
Consultant Medical Oncology - Colorectal Oncology
The Christie NHS FT
Greater Manchester, North West England
GBP 113,565 - 150,569 per year
Gynaecologist
Job summary This post is for 8 Programmed Activities (PAs) per week to work within the Medical Oncology Colorectal Disease Group mainly based at The Christie s…
1 month(s) ago
Clinical Research Practitioner
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary We're looking for a full time Band 5 Clinical Research Practitioner to coordinate and deliver clinical research studies at The Christie NHS Foundat…
1 month(s) ago
Clinical Research Practitioner
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary We're looking for a full time Band 5 Clinical Research Practitioner to coordinate and deliver clinical research studies at The Christie NHS Foundat…
1 month(s) ago
Radiopharmaceutical Technologist/Technician
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary We are looking for an enthusiastic and motivated Radiopharmaceutical Technologist with experience in aseptic dispensing to join our dynamic and exp…
1 month(s) ago
Radiopharmaceutical Technologist/Technician
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary We are looking for an enthusiastic and motivated Radiopharmaceutical Technologist with experience in aseptic dispensing to join our dynamic and exp…
1 month(s) ago
Senior Clinical Trials Coordinator
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary This is an exciting opportunity to join the Advanced Immune and Cellular Therapy (AICT) Team at The Christie NHS Foundation Trust; an international…
1 month(s) ago
Senior Clinical Trials Coordinator
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary This is an exciting opportunity to join the Advanced Immune and Cellular Therapy (AICT) Team at The Christie NHS Foundation Trust; an international…
1 month(s) ago
Specialist Nutrition Support Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Radiographer
Job summary We have an exciting opportunity for an experienced and driven registered nurse to join our Specialist Nutrition Support Nurse team (band 6, 37.
1 month(s) ago
Specialist Nutrition Support Nurse
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Radiographer
Job summary We have an exciting opportunity for an experienced and driven registered nurse to join our Specialist Nutrition Support Nurse team (band 6, 37.
1 month(s) ago
Sponsorship Governance Facilitator
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Medical Researcher
Job summary We are seeking a Sponsorship Governance Facilitator to join the Sponsorship Team within the R&I Office at the Christie NHS Foundation Trust.
1 month(s) ago
Sponsorship Governance Facilitator
The Christie NHS FT
Greater Manchester, North West England
GBP 39,959 - 48,117 per year
Medical Researcher
Job summary We are seeking a Sponsorship Governance Facilitator to join the Sponsorship Team within the R&I Office at the Christie NHS Foundation Trust.
1 month(s) ago
Senior Clinical Pharmacy Technician
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary Pharmacy technicians from community, prison, PCNs or other settings, are encouraged to apply.
1 month(s) ago
Senior Clinical Pharmacy Technician
The Christie NHS FT
Greater Manchester, North West England
GBP 32,073 - 39,043 per year
Radiographer
Job summary Pharmacy technicians from community, prison, PCNs or other settings, are encouraged to apply.
1 month(s) ago
Posted 10 day(s) ago
Reference: 413-108084-CSSS-RS
Job summary
We have an exciting opportunity for an experienced and driven registered nurse to join our Specialist Nutrition Support Nurse team (band 6, 26.25 hrs/week), as part of the Christie nutrition and dietetic team in our world class cancer centre, providing an opportunity to develop your practice within this specialist area of nursing.
If you are you passionate and have and interest or experience of working within in nutrition and/or oncology, and experience of varied feeding tubes, such as gastrostomies, nasogastric tubes, nasojejunal tubes and want to develop your skills further, then this is the post for you. The experienced and well-established team will support with competency and confidence development for this specialist role.
As a member of the Specialist Nutrition Support Nurse team, you will work closely with the dietetic team, and, as well as collaborate with the wider MDT and stake holders, to deliver high quality patient centred care for patients requiring artificial nutrition.
Main duties of the job
As a band 6 Specialist Nutrition Support Nurse you will work within the team to provide a specialist nutrition support nurse service for patients aimed at continually improving standards of care and facilitating a multidisciplinary team approach.
You will participate in the nurse management of patients receiving artificial nutrition support via enteral feeding, utilising both gastrostomies, jejunostomies, nasogastric and nasojejunal routes, as well as supporting patients through the HPN (Home Parenteral nutrition) referral process, and provision of venting gastrojejunostomy support for some of these patients.
Working with the team you will ensure the nutritional needs of patients are met, providing counselling, tube training, tube placement/replacement, follow-up/aftercare for patients receiving artificial nutrition support, this includes supporting the gastrostomy drop clinic in conjunction with the nursing team.
You will work alongside the specialist nutrition support nurse team in the development and delivery of education and training programmes for health care professionals in the Trust and at regional level on nursing related nutritional care.
You will be an active member of the wider Nutrition and Dietetic team, and an active role model for the service. Within this role you will work closely with the wider MDT and external agencies to ensure national nutritional performance and clinical standards are met.
Please see job description for full duties.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
22 September 2026
Pay scheme
Agenda for change
Band
Band 6
Salary
£39,959 to £48,117 a year Per annum, Pro rata
Contract
Permanent
Working pattern
Part-time
Reference number
413-108084-CSSS-RS
Job locations
Dietetic Nursing - E00975
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
Clinical1. To support the senior nutrition nurse and be responsible for own caseload providing an expert assessment plan and evaluation within the specialist area for enteral tubes2. To conduct regular ward visits to ensure compliance with nutritional standards and act as a resource for nutrition care planning and feeding tubes care delivery.3. To be involved in patient selection and education regarding enteral and parenteral nutrition support.4. To attend multidisciplinary / best interest meetings to discuss management of patients requiring enteral or parenteral nutrition at home.5. To maintain accurate, comprehensive and up to date documentation on the patient electronic system of individual patients in line with local and national standards and trust policy on confidentiality.6. To cover and support the organisation of home parenteral nutrition feed discharge patients as required alongside other nutrition nurse colleagues
Enteral7. To counsel and educate patients during the consent process for placement of enteral feeding tubes.8. To be competent to place nasogastric feeding tubes.9. To coordinate the gastrostomy service in collaboration with the senior nutrition nurse and interventional radiology team.10. To provide follow-up after interventional procedures for nutritional support and help with audit of outcome data.11. To be able to place secondary gastrostomy tube devices in hospital.12. To work alongside the dietitians and be involved in the setting up of a home enteral feed to ensure a safe and timely discharge.13. To educate and support the patient, carers, nursing staff and district nurses on the care of enteral feeding tubes before and after discharge.14. To work with the senior nutrition nurse to develop the nutritional nursing care service to patients in line with national standards.15. To work closely with the nutrition nurse teams, dietitians, nurse leaders and nurse clinicians to promote good practice and lead and support changes in practice16. To take an active role in audit and annually supporting the review of nursing guidelines, policies and patient information concerning enteral and parenteral nutrition in conjunction with the dietitians and senior nutrition nurse.17. To identify clinical issues and incidents within the Trust that reduces the quality of care within the specialist service. Devise strategies to counter these to ensure the delivery of safe and effective care.18. To maintain patient data and statistics for service development19. To attend and participate in departmental, professional update meetings and trust nutrition related meetings.20. To be responsible for own clinical professional development (CPD) to maintain competency and to ensure best practice.21. Take an active part in professional networks to ensure the exchange of knowledge and ideas, both locally and nationally. Contribute to the development of national policy.22. In conjunction with the senior nutrition nurse provide specialist nursing knowledge of nutritional care to medical and nursing staff and students23. In conjunction with the senior nutrition nurse deliver an education programme on the nurse management of oncology patients receiving nutrition support internally and externally at regional level to nursing staff and other health care professionals.24. To work with the senior nutrition nurse to develop the nutrition link nurse group and be accountable to the Nutrition steering group.25. To promote good nursing practice in enteral and parenteral feeding to ward staff.26. To participate in the education of nursing staff on nutritionally screening patients, care planning and protected mealtimes and carry out regular audits.
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
Clinical1. To support the senior nutrition nurse and be responsible for own caseload providing an expert assessment plan and evaluation within the specialist area for enteral tubes2. To conduct regular ward visits to ensure compliance with nutritional standards and act as a resource for nutrition care planning and feeding tubes care delivery.3. To be involved in patient selection and education regarding enteral and parenteral nutrition support.4. To attend multidisciplinary / best interest meetings to discuss management of patients requiring enteral or parenteral nutrition at home.5. To maintain accurate, comprehensive and up to date documentation on the patient electronic system of individual patients in line with local and national standards and trust policy on confidentiality.6. To cover and support the organisation of home parenteral nutrition feed discharge patients as required alongside other nutrition nurse colleagues
Enteral7. To counsel and educate patients during the consent process for placement of enteral feeding tubes.8. To be competent to place nasogastric feeding tubes.9. To coordinate the gastrostomy service in collaboration with the senior nutrition nurse and interventional radiology team.10. To provide follow-up after interventional procedures for nutritional support and help with audit of outcome data.11. To be able to place secondary gastrostomy tube devices in hospital.12. To work alongside the dietitians and be involved in the setting up of a home enteral feed to ensure a safe and timely discharge.13. To educate and support the patient, carers, nursing staff and district nurses on the care of enteral feeding tubes before and after discharge.14. To work with the senior nutrition nurse to develop the nutritional nursing care service to patients in line with national standards.15. To work closely with the nutrition nurse teams, dietitians, nurse leaders and nurse clinicians to promote good practice and lead and support changes in practice16. To take an active role in audit and annually supporting the review of nursing guidelines, policies and patient information concerning enteral and parenteral nutrition in conjunction with the dietitians and senior nutrition nurse.17. To identify clinical issues and incidents within the Trust that reduces the quality of care within the specialist service. Devise strategies to counter these to ensure the delivery of safe and effective care.18. To maintain patient data and statistics for service development19. To attend and participate in departmental, professional update meetings and trust nutrition related meetings.20. To be responsible for own clinical professional development (CPD) to maintain competency and to ensure best practice.21. Take an active part in professional networks to ensure the exchange of knowledge and ideas, both locally and nationally. Contribute to the development of national policy.22. In conjunction with the senior nutrition nurse provide specialist nursing knowledge of nutritional care to medical and nursing staff and students23. In conjunction with the senior nutrition nurse deliver an education programme on the nurse management of oncology patients receiving nutrition support internally and externally at regional level to nursing staff and other health care professionals.24. To work with the senior nutrition nurse to develop the nutrition link nurse group and be accountable to the Nutrition steering group.25. To promote good nursing practice in enteral and parenteral feeding to ward staff.26. To participate in the education of nursing staff on nutritionally screening patients, care planning and protected mealtimes and carry out regular audits.
Person Specification
Qualifications
Essential
- Current NMC registration
- Diploma or degree in nursing studies
Desirable
- Mentorship module
Experience
Essential
- Experience in an acute setting NHS experience
- Experience in oncology
- Evidence of clinical audit
- Evidence of educational study in nutrition
- Evidence of interest in nutrition
- Evidence in recent management and care of patients with feeding tubes
Desirable
- Evidence of setting standards and producing action plans
- Experience in endoscopic / radiological procedures
- Experience in gastroenterology
Skills
Essential
- Able to deliver a high standard of evidence based individual patient care
- To provide all nursing care in line with Trust policies and protocols
- Good interpersonal skills and initiative.
- Able to work as part of a team Independently insert nasogastric tube
- Ability to train patients/carers for enteral tube care
- Assess gastrostomy tubes
- Provide aftercare for feeding tubes
- Able to teach formally and informally
- Able to present information written and verbal
- Computer literate
Desirable
- Replace gastrostomy tubes
Knowledge
Essential
- Up to date knowledge of nursing issues in relation to nutritional support, enteral feeding and parenteral feeding
- Understanding of national nutrition standards and guidelines (CQC, NPSA, PLACE, NICE)
- Knowledge of endoscopic and radiologic procedures for nutritional support
- Evidence of own personal continuing professional development (CPD)
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Able to work as autonomous practitioner
- Able to manage own workload
Person Specification
Qualifications
Essential
- Current NMC registration
- Diploma or degree in nursing studies
Desirable
- Mentorship module
Experience
Essential
- Experience in an acute setting NHS experience
- Experience in oncology
- Evidence of clinical audit
- Evidence of educational study in nutrition
- Evidence of interest in nutrition
- Evidence in recent management and care of patients with feeding tubes
Desirable
- Evidence of setting standards and producing action plans
- Experience in endoscopic / radiological procedures
- Experience in gastroenterology
Skills
Essential
- Able to deliver a high standard of evidence based individual patient care
- To provide all nursing care in line with Trust policies and protocols
- Good interpersonal skills and initiative.
- Able to work as part of a team Independently insert nasogastric tube
- Ability to train patients/carers for enteral tube care
- Assess gastrostomy tubes
- Provide aftercare for feeding tubes
- Able to teach formally and informally
- Able to present information written and verbal
- Computer literate
Desirable
- Replace gastrostomy tubes
Knowledge
Essential
- Up to date knowledge of nursing issues in relation to nutritional support, enteral feeding and parenteral feeding
- Understanding of national nutrition standards and guidelines (CQC, NPSA, PLACE, NICE)
- Knowledge of endoscopic and radiologic procedures for nutritional support
- Evidence of own personal continuing professional development (CPD)
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Able to work as autonomous practitioner
- Able to manage own workload
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Dietetic Nursing - E00975
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Dietetic Nursing - E00975
Manchester
M20 4BX
United Kingdom
Employer's website
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Posted 10 day(s) ago
Reference: 413-110653-CNS-LM
Job summary
An exciting opportunity has arisen for an experienced and motivated nurse to join the Clinical Apheresis Unit (CAU) within the Haematology and Transplant Day Unit as Apheresis Lead Nurse. The post will provide clinical leadership for the day-to-day delivery and development of a comprehensive nurse-led apheresis service for patients and donors. The successful candidate will coordinate the apheresis pathway, working closely with the Apheresis Director, Cellular Therapy Programme, transplant and donor coordinators and the wider multidisciplinary team. You will provide expert nursing care for patients undergoing stem cell and lymphocyte collection, support safe and effective service delivery, and contribute to quality improvement, education, competency development and service expansion. Experience in apheresis is essential and with knowledge in haematology/oncology, & transplant, cellular therapy. You will need strong clinical judgement, leadership, organisation and communication skills and the ability to work collaboratively in a highly specialist service.
Main duties of the job
You will lead and coordinate the day-to-day clinical delivery of the apheresis service, ensuring safe, effective and patient-centred care for patients and donors. You will assess and prioritise service requirements, coordinate patient and donor scheduling, and work collaboratively with transplant, donor and cellular therapy teams to manage the complete apheresis pathway. You will provide expert assessment and management of patients during apheresis, including recognition and escalation of clinical deterioration and troubleshooting of procedural issues. You will promote high standards of practice in line with the NMC Code, The Christie policies, JACIE and HTA requirements. You will support governance, audit, risk management and continuous improvement, contribute to the development and review of SOPs, and help ensure appropriate documentation and traceability. You will lead and support staff education, induction and competency assessment, working with external training providers where required. You will contribute to service planning and development as activity grows, working with the Apheresis Director and wider team to identify opportunities to improve efficiency, patient experience and clinical outcomes.
About us
The Clinical Apheresis Unit is a specialist service embedded within the Haematology and Transplant Day Unit, caring for patients with haematological malignancies, lymphoma and teenage and young adult patients, as well as related and unrelated donors. You will work alongside an established multidisciplinary team and have a key role in developing the nurse-led apheresis service as activity continues to expand. The role offers the opportunity to develop and use specialist knowledge in apheresis, stem cell collection, lymphocyte collection, cellular therapy and transplant pathways. We value collaborative working, professional development and a strong focus on safe, high-quality patient care. Training and support will be provided, including specialist apheresis training and opportunities to develop leadership, education and service-improvement skills. Working hours are Monday to Friday, between 08:00 and 18:00, 37.5 hours per week.
Details
Date posted
22 September 2026
Pay scheme
Agenda for change
Band
Band 7
Salary
£49,387 to £56,515 a year Pro rata Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-110653-CNS-LM
Job locations
Haematology Specialist Nursing - E00286
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
1. CLINICAL PRACTICE
Provide a specialist nursing service for patients and donors undergoing clinical apheresis, using advanced specialist knowledge, clinical judgement and decision-making to deliver safe, effective and individualised care.
Provide timely written and verbal information, advice and support to patients, donors and relatives to facilitate informed consent, shared decision-making and understanding of the apheresis pathway.
Maintain current specialist knowledge of clinical apheresis and cellular therapy collection procedures, relevant protocols, standards and practices, and apply this knowledge to clinical care and service development.
Coordinate and plan apheresis treatment pathways with members of the multidisciplinary team, including internal and external services, to ensure procedures are appropriately scheduled and communicated.
Lead the day-to-day clinical apheresis service, including autonomous management of a designated patient caseload and undertaking apheresis procedures as required.
Liaise directly with the consultant medical team regarding the assessment, planning, implementation and evaluation of individual programmes of care and apheresis protocols.
Participate in outpatient clinics and support medical assessment of patients requiring apheresis, including assessment of venous access, confirmation of mobilisation and collection requirements, and communication of the planned pathway to relevant teams.
Ensure all documentation required for apheresis procedures is prepared and completed in a timely manner in accordance with departmental requirements and regulatory standards.
Work with the quality and data manager to maintain accurate records, collect relevant activity and outcome data, support service evaluation and contribute to change and improvement.
Develop, implement and review clinical apheresis policies, procedures and protocols, and participate in clinical audit, regulatory accreditation activity, annual reporting and quality manual development, including JACIE and HTA requirements.
Proactively review trial and commercial documentation relating to apheresis procedures and participate in relevant meetings to ensure requirements are understood and incorporated into the clinical pathway.
2. EDUCATION
Act as an expert resource within the organisation in the field of apheresis and cellular therapy collections, providing advice and support to the multidisciplinary team.
Plan and deliver training and education relating to apheresis and associated practice for members of the multidisciplinary team within and external to the Trust.
Coordinate the training, orientation and competency assessment of members of the clinical apheresis team, ensuring appropriate support and supervision are available.
Promote the professional development of staff within the clinical apheresis team and support the identification and achievement of learning needs.
Maintain own professional development and ensure mandatory and role-specific education and training requirements are met.
Represent the organisation and department nationally and internationally as an expert in cellular therapy collections, as appropriate.
3. LEADERSHIP AND MANAGEMENT
Manage the clinical apheresis nursing and nursing team in collaboration with the providing visible professional leadership and acting as a role model.
Provide confident management, leadership and specialist advice to staff within areas of responsibility, supporting effective communication, teamwork and safe practice.
Lead the development and implementation of standards for clinical apheresis practice and patient care, ensuring that standards are monitored and audited.
Lead planning meetings with medical and laboratory colleagues to coordinate the apheresis programme in conjunction with cellular therapy and donor coordinators.
Coordinate the scheduling of apheresis procedures and contribute to effective capacity planning and communication across the patient pathway.
Work within agreed budgetary constraints and support efficient procurement and management of clinical stocks, equipment and resources.
Ensure team objectives and key performance indicators are established and that mechanisms are in place to demonstrate compliance, activity and performance.
Contribute to human resource management, recruitment and implementation of relevant Trust human resource policies for staff within the service.
4. RESEARCH
Maintain current knowledge of relevant research and evidence relating to apheresis, cellular therapy collections and specialist nursing practice.
Support the application and evaluation of research findings to promote quality, evidence-based clinical practice.
Develop research interests within the specialist field of clinical apheresis and cellular therapy collections.
Participate, as required, in research and audit undertaken by members of the multidisciplinary team.
Review apheresis-related research applications in relation to established clinical practice, standards and service requirements
5. PROFESSIONAL AND PERSONAL
Communicate professionally and courteously with patients, donors, relatives, colleagues and external stakeholders, using effective communication skills at all levels.
Demonstrate leadership by example through clear, fair and professional relationships with colleagues, sound organisation and effective clinical judgement.
Recognise and work within the limits of own professional competence, maintain confidentiality and practise in accordance with the NMC Code and relevant Trust policies.
Participate fully in performance review, identifying learning goals, development needs and support requirements.
Actively seek and engage in appropriate mentorship and professional supervision to support reflection and development, and provide supervision and support to colleagues.
Demonstrate the agreed Trust values and behaviours and take accountability for own attitude, conduct and professional behaviour.
Job description
Job responsibilities
1. CLINICAL PRACTICE
Provide a specialist nursing service for patients and donors undergoing clinical apheresis, using advanced specialist knowledge, clinical judgement and decision-making to deliver safe, effective and individualised care.
Provide timely written and verbal information, advice and support to patients, donors and relatives to facilitate informed consent, shared decision-making and understanding of the apheresis pathway.
Maintain current specialist knowledge of clinical apheresis and cellular therapy collection procedures, relevant protocols, standards and practices, and apply this knowledge to clinical care and service development.
Coordinate and plan apheresis treatment pathways with members of the multidisciplinary team, including internal and external services, to ensure procedures are appropriately scheduled and communicated.
Lead the day-to-day clinical apheresis service, including autonomous management of a designated patient caseload and undertaking apheresis procedures as required.
Liaise directly with the consultant medical team regarding the assessment, planning, implementation and evaluation of individual programmes of care and apheresis protocols.
Participate in outpatient clinics and support medical assessment of patients requiring apheresis, including assessment of venous access, confirmation of mobilisation and collection requirements, and communication of the planned pathway to relevant teams.
Ensure all documentation required for apheresis procedures is prepared and completed in a timely manner in accordance with departmental requirements and regulatory standards.
Work with the quality and data manager to maintain accurate records, collect relevant activity and outcome data, support service evaluation and contribute to change and improvement.
Develop, implement and review clinical apheresis policies, procedures and protocols, and participate in clinical audit, regulatory accreditation activity, annual reporting and quality manual development, including JACIE and HTA requirements.
Proactively review trial and commercial documentation relating to apheresis procedures and participate in relevant meetings to ensure requirements are understood and incorporated into the clinical pathway.
2. EDUCATION
Act as an expert resource within the organisation in the field of apheresis and cellular therapy collections, providing advice and support to the multidisciplinary team.
Plan and deliver training and education relating to apheresis and associated practice for members of the multidisciplinary team within and external to the Trust.
Coordinate the training, orientation and competency assessment of members of the clinical apheresis team, ensuring appropriate support and supervision are available.
Promote the professional development of staff within the clinical apheresis team and support the identification and achievement of learning needs.
Maintain own professional development and ensure mandatory and role-specific education and training requirements are met.
Represent the organisation and department nationally and internationally as an expert in cellular therapy collections, as appropriate.
3. LEADERSHIP AND MANAGEMENT
Manage the clinical apheresis nursing and nursing team in collaboration with the providing visible professional leadership and acting as a role model.
Provide confident management, leadership and specialist advice to staff within areas of responsibility, supporting effective communication, teamwork and safe practice.
Lead the development and implementation of standards for clinical apheresis practice and patient care, ensuring that standards are monitored and audited.
Lead planning meetings with medical and laboratory colleagues to coordinate the apheresis programme in conjunction with cellular therapy and donor coordinators.
Coordinate the scheduling of apheresis procedures and contribute to effective capacity planning and communication across the patient pathway.
Work within agreed budgetary constraints and support efficient procurement and management of clinical stocks, equipment and resources.
Ensure team objectives and key performance indicators are established and that mechanisms are in place to demonstrate compliance, activity and performance.
Contribute to human resource management, recruitment and implementation of relevant Trust human resource policies for staff within the service.
4. RESEARCH
Maintain current knowledge of relevant research and evidence relating to apheresis, cellular therapy collections and specialist nursing practice.
Support the application and evaluation of research findings to promote quality, evidence-based clinical practice.
Develop research interests within the specialist field of clinical apheresis and cellular therapy collections.
Participate, as required, in research and audit undertaken by members of the multidisciplinary team.
Review apheresis-related research applications in relation to established clinical practice, standards and service requirements
5. PROFESSIONAL AND PERSONAL
Communicate professionally and courteously with patients, donors, relatives, colleagues and external stakeholders, using effective communication skills at all levels.
Demonstrate leadership by example through clear, fair and professional relationships with colleagues, sound organisation and effective clinical judgement.
Recognise and work within the limits of own professional competence, maintain confidentiality and practise in accordance with the NMC Code and relevant Trust policies.
Participate fully in performance review, identifying learning goals, development needs and support requirements.
Actively seek and engage in appropriate mentorship and professional supervision to support reflection and development, and provide supervision and support to colleagues.
Demonstrate the agreed Trust values and behaviours and take accountability for own attitude, conduct and professional behaviour.
Person Specification
Qualifications
Essential
- Registered Nurse with current NMC registration
- Evidence of relevant specialist education/training in haematology, apheresis, cellular therapy
Desirable
- Oncology/Haematology or transplant related courses
- Non-medical prescribing
- Working towards a masters in a health-related subject
Experience
Essential
- Substantial post-registration experience in Adult Haematology and/or cellular therapy
- Extensive experience of Clinical Apheresis and Cellular therapy collections
- Experience of coordinating complex patient pathways and working across multidisciplinary teams
- Experience of clinical leadership, staff support, training and competency assessment
Desirable
- Experience of supporting research activity within specialist practice
- Experience of audit, quality improvement, policy/protocol development and regulatory/accreditation requirements
Skills
Essential
- Trained in Apheresis
- Excellent communication and interpersonal skills
- IT skills
- Leadership and Management
- Decision making
Desirable
- Advanced Communication course
Knowledge
Essential
- Therapeutic Apheresis
- Cellular therapies processes and stem cell transplantation
Desirable
- Knowledge of current research and emerging developments in apheresis and cellular therapy
- Knowledge of research governance and study processes
Values
Essential
- Ability to demonstrate the organisational values and behaviours
- Demonstrates professional, respectful, inclusive and patient-centred practice
Person Specification
Qualifications
Essential
- Registered Nurse with current NMC registration
- Evidence of relevant specialist education/training in haematology, apheresis, cellular therapy
Desirable
- Oncology/Haematology or transplant related courses
- Non-medical prescribing
- Working towards a masters in a health-related subject
Experience
Essential
- Substantial post-registration experience in Adult Haematology and/or cellular therapy
- Extensive experience of Clinical Apheresis and Cellular therapy collections
- Experience of coordinating complex patient pathways and working across multidisciplinary teams
- Experience of clinical leadership, staff support, training and competency assessment
Desirable
- Experience of supporting research activity within specialist practice
- Experience of audit, quality improvement, policy/protocol development and regulatory/accreditation requirements
Skills
Essential
- Trained in Apheresis
- Excellent communication and interpersonal skills
- IT skills
- Leadership and Management
- Decision making
Desirable
- Advanced Communication course
Knowledge
Essential
- Therapeutic Apheresis
- Cellular therapies processes and stem cell transplantation
Desirable
- Knowledge of current research and emerging developments in apheresis and cellular therapy
- Knowledge of research governance and study processes
Values
Essential
- Ability to demonstrate the organisational values and behaviours
- Demonstrates professional, respectful, inclusive and patient-centred practice
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Haematology Specialist Nursing - E00286
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Haematology Specialist Nursing - E00286
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
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Posted 10 day(s) ago
Reference: 413-110647-RI-DA
Job summary
This post is offered at 37.5 hours per week but we are happy to access flexible working or part time working requests.
We are looking to appoint a Clinical Trials Assistant (Band 3) in the Renal and Oesophagogastric Research team within The Christie NHS Foundation Trust. The role has scope to transition to that of a Clinical Trials Coordinator (Band 4) following successful completion of a competency review. The research teams form part of the Research and Innovation division and are made up of a multi-disciplinary group of staff who are dedicated to cancer research and treatment.
We are seeking an enthusiastic and motivated individual who will be responsible for assisting the research nurses, consultants and trial coordination management team with various aspects of clinical trial administration/ coordination.
Applicants should meet all the essential criteria on the job description as a minimum. We are looking for a candidate with good organisational and communication skills, with the ability to multi-task. Due to the vital nature of our work and the impact on patients and the research community, attention to detail is an essential skill.
For further specific information on this post, please contact:Amna Khawaja (Research Portfolio Manager) [email protected]
Main duties of the job
The administrative team members each manage a portfolio of clinical trials with support from other colleagues. The day-to-day role includes entering data from patient visits, responding to trial queries, completing trial-related records, filing key trial documents, assisting with invoicing, working with members of the core Research and Innovation team, liaising with pharmaceutical contacts, and assisting colleagues with other administrative tasks.
We have a strong team working ethos and you will be required to work closely with different members of staff. The Clinical Trials Assistant / Coordinator role comes with full training, and the opportunity for additional training to support career development within the Trust.The Renal and Oesophagogastric team works on studies including early phase, biomarker trials, real-world data, radiotherapy and will eventually be involved in innovative proton beam trials. The Christie's research teams contribute towards pioneering research and innovation and we constantly work towards improving cancer care and patient outcomes. A role within our team is challenging but rewarding; we are a hard-working and friendly team with a passion for research and patient care.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
22 September 2026
Pay scheme
Agenda for change
Band
Band 3
Salary
£25,760 to £31,157 a year Pro Rata, Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-110647-RI-DA
Job locations
Renal - Q01128
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
The specific responsibilities will depend on the requirements of each team, but may include:
Act as a point of contact for the Research and Development core team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to general trial conduct. Assist with the general administrative duties associated with the set up and initiation of rials within an assigned team, under the supervision of the Senior Clinical Trials Coordinators.
Assist with completion of activity logs to enable invoices to be raised. Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times.
Assist with the processing of trial amendment submissions in accordance with ICH GCP and Trust SOPs and timelines, under the supervision of the Senior Clinical Trials Coordinators.
Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety reporting in accordance with protocol requirements, under the supervision of the Senior Clinical Trials Coordinators.
Complete team reporting mechanisms (i.e. recruitment activity logs, patient visit logs, costing spreadsheets, case report form trackers and electronic proformas).
Assist the Clinical Trials Coordinators with the development of trial workbooks for review by the lead Clinical Research Nurse and Principal Investigator.
Ensure collection of clinical case notes for all patients, so that these are available as needed, for monitoring and audit purposes.
Complete case report forms as per sponsor requirements and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits. This will be under the supervision of the Senior Clinical Trials Coordinators.
Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature.
Arrange shipping and delivery of relevant trial data and documents including import/export of tumour blocks, ECGs and copy scans. Arrange team and trial related meetings as required, producing minutes in a timely manner.
Ensure that data is available and up to date for any meetings related to a clinical trial in collaboration with the Senior Clinical Trials Coordinators.
Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary).
Assist with general preparation for audit and inspections within assigned teams, under the direct supervision of the Senior Clinical Trials Coordinators and lead Clinical Research Nurse.
Assist with trial document archiving by following the Trusts archiving guidelines.
Ensure that office/ trial related supplies are adequate and assist with the ordering process.
Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment teams. Demonstrates the agreed set of values and accountable for own attitude and behaviour.
Job description
Job responsibilities
The specific responsibilities will depend on the requirements of each team, but may include:
Act as a point of contact for the Research and Development core team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to general trial conduct. Assist with the general administrative duties associated with the set up and initiation of rials within an assigned team, under the supervision of the Senior Clinical Trials Coordinators.
Assist with completion of activity logs to enable invoices to be raised. Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times.
Assist with the processing of trial amendment submissions in accordance with ICH GCP and Trust SOPs and timelines, under the supervision of the Senior Clinical Trials Coordinators.
Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety reporting in accordance with protocol requirements, under the supervision of the Senior Clinical Trials Coordinators.
Complete team reporting mechanisms (i.e. recruitment activity logs, patient visit logs, costing spreadsheets, case report form trackers and electronic proformas).
Assist the Clinical Trials Coordinators with the development of trial workbooks for review by the lead Clinical Research Nurse and Principal Investigator.
Ensure collection of clinical case notes for all patients, so that these are available as needed, for monitoring and audit purposes.
Complete case report forms as per sponsor requirements and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits. This will be under the supervision of the Senior Clinical Trials Coordinators.
Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature.
Arrange shipping and delivery of relevant trial data and documents including import/export of tumour blocks, ECGs and copy scans. Arrange team and trial related meetings as required, producing minutes in a timely manner.
Ensure that data is available and up to date for any meetings related to a clinical trial in collaboration with the Senior Clinical Trials Coordinators.
Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary).
Assist with general preparation for audit and inspections within assigned teams, under the direct supervision of the Senior Clinical Trials Coordinators and lead Clinical Research Nurse.
Assist with trial document archiving by following the Trusts archiving guidelines.
Ensure that office/ trial related supplies are adequate and assist with the ordering process.
Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment teams. Demonstrates the agreed set of values and accountable for own attitude and behaviour.
Person Specification
Qualifications
Essential
- Diploma or administration experience
Desirable
- Degree in a science or health related discipline
Experience
Essential
- Experience of administrative tasks including data management
Desirable
- Previous experience of working within a clinical trials or research environment
- Experience of working within a health care system
Skills
Essential
- Good written and oral communication skills
- Accuracy and attention to detail
- Good understanding and demonstrated use of Microsoft Word and Excel
- Good organisational skills
- Good interpersonal skills
Desirable
- Good understanding and demonstrated use of the full Microsoft Office suite
Knowledge
Essential
- Some understanding of the clinical trials process
Desirable
- Understanding of medical terminology and cancer.
- Knowledge of patient information systems
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Flexible With ability to adapt to service requirements
- Hardworking; ability to manage a busy workload
- Ability to work unsupervised or as part of a team
Desirable
- Ability to work to tight and/or unexpected deadlines
Person Specification
Qualifications
Essential
- Diploma or administration experience
Desirable
- Degree in a science or health related discipline
Experience
Essential
- Experience of administrative tasks including data management
Desirable
- Previous experience of working within a clinical trials or research environment
- Experience of working within a health care system
Skills
Essential
- Good written and oral communication skills
- Accuracy and attention to detail
- Good understanding and demonstrated use of Microsoft Word and Excel
- Good organisational skills
- Good interpersonal skills
Desirable
- Good understanding and demonstrated use of the full Microsoft Office suite
Knowledge
Essential
- Some understanding of the clinical trials process
Desirable
- Understanding of medical terminology and cancer.
- Knowledge of patient information systems
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Flexible With ability to adapt to service requirements
- Hardworking; ability to manage a busy workload
- Ability to work unsupervised or as part of a team
Desirable
- Ability to work to tight and/or unexpected deadlines
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Renal - Q01128
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Renal - Q01128
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 10 day(s) ago
Reference: 413-110466-CSSS-TM
Job summary
The Integrated Procedures Unit (IPU) has an exciting opportunity for a highly motivated, organised and competent Staff Nurse to join our core nursing team.
This role is for 37.5 hours per week, worked over 4 days for a fixed term initially of 12 months. IPU is open 07:30-19:30 Monday to Friday, so this is a great opportunity to achieve an excellent work-life balance whilst joining a dynamic nurse-led service.
Please note, you must have a valid and current NMC PIN to apply for this post. Please do not apply if you have not got a UK NMC PIN and are unable to practise immediately as a Registered Nurse.
Main duties of the job
The Post holder will be responsible for the assessment, planning and evaluating care for patients on the Unit and on the DOSA. The post holder will admit patients for all treatments within the unit in the admissions area. The post holder will provide second stage recovery for GA and LA, endoscopy and interventional radiology and procedures team and day case patients. The post holder will rotate into the endoscopy room and nurse lead dressings clinic and DOSA. They will provide a high standard of clinical nursing within the IPU and manage a group of patients. They will act as a role model to students and Clinical Support Workers and present a positive, professional image of the organisation and of the nursing team.
About us
The Christie is an internationally and nationally recognised Centre for the treatment of cancer and we are leading experts in cancer care, research and education based in Manchester.
The Integrated Procedures Unit (IPU) is a nurse-led, fast-paced and dynamic service. The unit consists of a procedures unit, interventional radiology unit, ultrasound room, surgical dressings clinic, outpatients clinic, day of surgery admissions unit, an operating theatre and second stage recovery bays.
You will become part of this complex multidisciplinary team and benefit from a comprehensive induction period.
Details
Date posted
22 September 2026
Pay scheme
Agenda for change
Band
Band 5
Salary
£32,073 to £39,043 a year per annum, pro rata
Contract
Fixed term
Duration
12 months
Working pattern
Full-time
Reference number
413-110466-CSSS-TM
Job locations
Integrated Procedures Unit - E00326
Wilmslow Road
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
- To participate as a member of the IPU core nursing team with knowledge in the care of the patients on the unit.
- To demonstrate high standards of individual patient care with a commitment to the development of evidence-based practice.
- To competently care for the patient including the assessment, planning and evaluation of programs of care.
- Liaise and integrate with the multi-disciplinary team, ensuring patients receive comprehensive care and promote a team approach to working.
- Develop good working relationships and promote effective communication between all clinical grades of staff within the multi-disciplinary IPU team.
- The post holder will be proactive towards change and change management.
- Take responsibility for your own professional development.
- To monitor the progress of learners and in particular their skills in carrying out practical procedures.
- Demonstrate professional accountability.
- Act as a clinical role model for new staff, reflecting the philosophy, beliefs and standards of the department.
- Ensure that all prescribed drugs and treatments are given correctly and in accordance with Trust policy, including the correct care and custody of controlled drugs.
- Offer help and advice to the patients relatives and friends responding to their individual needs in a caring supportive manner.
- Ensure safe use and efficient management of equipment and supplies.
- Communicate using a range of methods to ensure a caring, sensitive and empathetic manner to patients and their relatives.
- Provide clear and concise patient handover to other members of the team.
- To participate as a member of the IPU team with knowledge in the care of the patients on the unit.
- To competently care for the patient including the assessment, planning and evaluation of programs of care.
- Liaise and integrate with the multi-disciplinary team, ensuring patients receive comprehensive care and promote a team approach to working.
- Demonstrate respect for the individual patient, ensuring religious, cultural and social needs are considered at all times and acknowledge their individual rights. In all situations ensure consideration is made to the patients cultural background.
- Recognises peoples differences and act in a non-discriminatory way.
- Recognise and report abusive behaviour to an appropriate member of staff. Document same. Liaise, communicate and negotiate with colleagues to ensure co-operation in achieving departmental objectives, promoting good working relationships and establishing team spirit. Contribute to effective team working, by being fully involved, committed and participative to achieving full potential.
Take responsibility for your own professional development.Rotate onto the day of surgery admissions unit.Rotate into the endoscopy unit.Rotate into the nurse lead dressings clinics.Escalate concerns in a patients condition to senior members of the nursing team, medical staffInitiate referrals to other members of the healthcare team.To report departmental affairs to the Sister / Charge Nurse.Can priorities workload to manage the care for a group of patientsTo ensure that confidentiality is maintained at all times
Freedom to Act
Works autonomously. Required to act independently within appropriate guidelines, deciding when it is necessary to refer to their manager.
Physical Effort
Will be required to be able to undertake a range of manual procedures including assistance with the movement of patients and equipmentTo be able to manoeuvre between patients quickly to ensure emergency situations can be attended in a timely fashion.
Mental Effort
Ability to interpret complex information when there may be frequent, unplanned interruptions throughout the shift.
Infection Control
Infection Control is everyones responsibility. All staff, both clinical and non clinical, are required to adhere to the Trusts Infection Prevention and Control Policies and make every effort to maintain high standards of infection control at all times thereby reducing the burden of Healthcare Associated Infections including MRSA.
Safeguarding Children, Young People and the Vulnerable Adult
All staff are responsible for ensuring that they are familiar with and adhere
to the Trusts Safeguarding procedures and guidelines.
All staff are required to attend safeguarding awareness training and undertake any additional training in relation to safeguarding relevant to their role.
Clinical Governance, Audit, Research and Development
- Work within trust guidelines, policies and standard operating procedures.
- Utilise incident reporting system.
- Support patient and public involvement activities in the IPU and DOSA area as appropriate, leading to service improvement
- Ensure compliance with untoward incident reporting & near misses
- Promote peoples equality, diversity and rights. Assist the IPU Matron in the effective use and monitoring the quality of supplies / equipment
- To take reasonable care for your own Health and Safety and that of any other person who may be affected by your acts or omissions at work.
- Be responsible for the assessment of needs, development, implementation and evaluation of programmes of patient care in line with the Nursing and Midwifery Council (NMC) code of Professional Conduct and reflect the Trusts policies, procedures, standards and guidelines.
Finance/ Physical Resources
- Responsible for the security and safe use of all Trust equipment.
- To be responsible for the maintenance of equipment within the Unit and on DOSA with regular checking of all equipment and ensuring that repairs are performed as soon as possible.
- Assist in the management of resources by participating in the selection, ordering and monitoring of departmental stock items.
- To ensure the safe keeping of patients property and valuables in line with Trust policy
- Assist the Matron to maintain IPU budgets and assist in cost saving projects
- Comply with best practice in the safe use of equipment by self and other members of the team, i.e. trainees / medical and nursing staff
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
- To participate as a member of the IPU core nursing team with knowledge in the care of the patients on the unit.
- To demonstrate high standards of individual patient care with a commitment to the development of evidence-based practice.
- To competently care for the patient including the assessment, planning and evaluation of programs of care.
- Liaise and integrate with the multi-disciplinary team, ensuring patients receive comprehensive care and promote a team approach to working.
- Develop good working relationships and promote effective communication between all clinical grades of staff within the multi-disciplinary IPU team.
- The post holder will be proactive towards change and change management.
- Take responsibility for your own professional development.
- To monitor the progress of learners and in particular their skills in carrying out practical procedures.
- Demonstrate professional accountability.
- Act as a clinical role model for new staff, reflecting the philosophy, beliefs and standards of the department.
- Ensure that all prescribed drugs and treatments are given correctly and in accordance with Trust policy, including the correct care and custody of controlled drugs.
- Offer help and advice to the patients relatives and friends responding to their individual needs in a caring supportive manner.
- Ensure safe use and efficient management of equipment and supplies.
- Communicate using a range of methods to ensure a caring, sensitive and empathetic manner to patients and their relatives.
- Provide clear and concise patient handover to other members of the team.
- To participate as a member of the IPU team with knowledge in the care of the patients on the unit.
- To competently care for the patient including the assessment, planning and evaluation of programs of care.
- Liaise and integrate with the multi-disciplinary team, ensuring patients receive comprehensive care and promote a team approach to working.
- Demonstrate respect for the individual patient, ensuring religious, cultural and social needs are considered at all times and acknowledge their individual rights. In all situations ensure consideration is made to the patients cultural background.
- Recognises peoples differences and act in a non-discriminatory way.
- Recognise and report abusive behaviour to an appropriate member of staff. Document same. Liaise, communicate and negotiate with colleagues to ensure co-operation in achieving departmental objectives, promoting good working relationships and establishing team spirit. Contribute to effective team working, by being fully involved, committed and participative to achieving full potential.
Take responsibility for your own professional development.Rotate onto the day of surgery admissions unit.Rotate into the endoscopy unit.Rotate into the nurse lead dressings clinics.Escalate concerns in a patients condition to senior members of the nursing team, medical staffInitiate referrals to other members of the healthcare team.To report departmental affairs to the Sister / Charge Nurse.Can priorities workload to manage the care for a group of patientsTo ensure that confidentiality is maintained at all times
Freedom to Act
Works autonomously. Required to act independently within appropriate guidelines, deciding when it is necessary to refer to their manager.
Physical Effort
Will be required to be able to undertake a range of manual procedures including assistance with the movement of patients and equipmentTo be able to manoeuvre between patients quickly to ensure emergency situations can be attended in a timely fashion.
Mental Effort
Ability to interpret complex information when there may be frequent, unplanned interruptions throughout the shift.
Infection Control
Infection Control is everyones responsibility. All staff, both clinical and non clinical, are required to adhere to the Trusts Infection Prevention and Control Policies and make every effort to maintain high standards of infection control at all times thereby reducing the burden of Healthcare Associated Infections including MRSA.
Safeguarding Children, Young People and the Vulnerable Adult
All staff are responsible for ensuring that they are familiar with and adhere
to the Trusts Safeguarding procedures and guidelines.
All staff are required to attend safeguarding awareness training and undertake any additional training in relation to safeguarding relevant to their role.
Clinical Governance, Audit, Research and Development
- Work within trust guidelines, policies and standard operating procedures.
- Utilise incident reporting system.
- Support patient and public involvement activities in the IPU and DOSA area as appropriate, leading to service improvement
- Ensure compliance with untoward incident reporting & near misses
- Promote peoples equality, diversity and rights. Assist the IPU Matron in the effective use and monitoring the quality of supplies / equipment
- To take reasonable care for your own Health and Safety and that of any other person who may be affected by your acts or omissions at work.
- Be responsible for the assessment of needs, development, implementation and evaluation of programmes of patient care in line with the Nursing and Midwifery Council (NMC) code of Professional Conduct and reflect the Trusts policies, procedures, standards and guidelines.
Finance/ Physical Resources
- Responsible for the security and safe use of all Trust equipment.
- To be responsible for the maintenance of equipment within the Unit and on DOSA with regular checking of all equipment and ensuring that repairs are performed as soon as possible.
- Assist in the management of resources by participating in the selection, ordering and monitoring of departmental stock items.
- To ensure the safe keeping of patients property and valuables in line with Trust policy
- Assist the Matron to maintain IPU budgets and assist in cost saving projects
- Comply with best practice in the safe use of equipment by self and other members of the team, i.e. trainees / medical and nursing staff
Person Specification
Qualifications
Essential
- RGN Level 1 or 2
- Degree or Diploma in Nursing Studies
- NMC valid PIN. Pre-Registration PIN number cannot be accepted
Desirable
- Post Graduate certificate in cancer care / oncology or acute care
- Post graduate certificate in teaching and assessing
Experience
Essential
- Experience in an acute care or oncology setting
Desirable
- Previous acute care/oncology experience
- Plastic dressing and recovery/ airway management experience
Skills
Essential
- Excellent communication skills
- Ability to deliver a high standard of nursing care
- Computer literacy
- Understanding need for evidence based practice
Desirable
- Cannulation/venepuncture skills
- ECG'S
Knowledge
Essential
- Participate in personal development
Person Specification
Qualifications
Essential
- RGN Level 1 or 2
- Degree or Diploma in Nursing Studies
- NMC valid PIN. Pre-Registration PIN number cannot be accepted
Desirable
- Post Graduate certificate in cancer care / oncology or acute care
- Post graduate certificate in teaching and assessing
Experience
Essential
- Experience in an acute care or oncology setting
Desirable
- Previous acute care/oncology experience
- Plastic dressing and recovery/ airway management experience
Skills
Essential
- Excellent communication skills
- Ability to deliver a high standard of nursing care
- Computer literacy
- Understanding need for evidence based practice
Desirable
- Cannulation/venepuncture skills
- ECG'S
Knowledge
Essential
- Participate in personal development
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Integrated Procedures Unit - E00326
Wilmslow Road
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Integrated Procedures Unit - E00326
Wilmslow Road
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
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Sign in to pre-fill your personal details, attachments and more.
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Posted 25 day(s) ago
Reference: 413-109167-CSSS-TM
Job summary
An exciting opportunity has arisen for an enthusiastic individual to become part of the Palliative and Supportive Care Teams, rotation will be required at times to cover other secretarial areas here at The Christie.
The successful candidate will provide a comprehensive and effective secretarial support service to the directorates' secretarial teams to assist with the day-to-day clinic management of the clinic templates. To ensure PA/secretarial duties are carried out to a high standard in order to meet patient needs and to ensure that Trust targets are always maintained. To keep accurate, up-to-date patient records; to type clinic annotations and letters and to help ensure that future appointments are made.
The successful candidate should have excellent communication skills, typing and be able to prioritise their workload.
Main duties of the job
Works closely with the clinical teams to provide comprehensive support for all clinical work within the directorate.
Work closely with clinicians to manage clinic templates including amending appointments slots, cancelling, reducing or adding new streams & adding ad hoc or new clinics onto the Patient Administration System (Careflow)
Audio typing of correspondence & results, ensuring tight turnaround times are met.
Is responsible for ensuring external correspondence is scanned efficiently into the patient electronic notes.
Appropriately disseminates a variety of correspondence/documentation across the department.
Ensures accurate input of patient details when entering data onto information databases & the patient administration system (Careflow).
Assists in ensuring timely delivery of notes to the appropriate department for out-patient appointments & in-patient admissions.
Assists in the registration of new patients to ensure they are seen within the cancer waiting time targets.
Exchange information with patients and staff on the admission & discharge of patients, both verbally & in written format.
Communicate with patients who may be anxious, angry or upset.
Exchange relevant information with GPs and other health professionals.Maintain patient confidentiality at all times.
Any other duties deemed necessary for the effective running of the services, & in accordance with the grade of this post.
Contributes to the training of new staff members within a given area as required
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
07 September 2026
Pay scheme
Agenda for change
Band
Band 3
Salary
£25,760 to £27,476 a year Pro Rata, Per Annum
Contract
Permanent
Working pattern
Part-time
Reference number
413-109167-CSSS-TM
Job locations
Central Administration - E00040
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
1. Works closely with the Medical Secretaries to provide comprehensive support for all clinical work within the directorate.2. Work closely with clinicians to manage clinic templates including amending appointments slots, cancelling, reducing or adding new streams and adding ad hoc or new clinics onto the Patient Administration System (Careflow)3. Audio typing of correspondence and results, ensuring tight turnaround times are met.4. Is responsible for ensuring external correspondence is scanned efficiently into the patient electronic notes.5. Appropriately disseminates a variety of correspondence/documentation across the department.6. Requests and obtains case notes and x-rays/scans both internally and from other hospitals, using the agreed procedures.7. Ensures accurate input of patient details when entering data onto information databases and the patient administration system (Careflow).8. Routinely uses the case note tracking system to ensure all patient case notes are tracked to their location.9. Support the Day Unit with the preparation of clinics.10. Provides cover in times of absence.11. Assists in ensuring timely delivery of notes to the appropriate department for out-patient appointments and in-patient admissions.12. Assists in the registration of new patients to ensure they are seen within the cancer waiting time targets.13. Exchange information with patients and staff on the admission and discharge of patients, both verbally and in written format.14. Communicate with patients who may be anxious, angry or upset.15. Exchange relevant information with GPs and other health professionals.16. Deal compassionately with distressing situations.17. Liaise with other members of staff regarding case notes and patient visits.18. Maintain patient confidentiality at all times.19. Always Remain professional when communicating with people in various situations.20. Undertakes other general office procedures, such as ordering stationery, opening and dispatching post, photocopying, printing etc.21. Any other duties deemed necessary for the effective running of the services, and in accordance with the grade of this post.22. Contributes to the training of new members of staff within a given area as required.23. Work with the Assistant Operations Manager and Secretaries to improve quality and range of services, with resources being managed according to agreed policies and priorities.24. To provide cross cover in periods of absence within the Administration Team and the wider Central Services Directorate
Job description
Job responsibilities
1. Works closely with the Medical Secretaries to provide comprehensive support for all clinical work within the directorate.2. Work closely with clinicians to manage clinic templates including amending appointments slots, cancelling, reducing or adding new streams and adding ad hoc or new clinics onto the Patient Administration System (Careflow)3. Audio typing of correspondence and results, ensuring tight turnaround times are met.4. Is responsible for ensuring external correspondence is scanned efficiently into the patient electronic notes.5. Appropriately disseminates a variety of correspondence/documentation across the department.6. Requests and obtains case notes and x-rays/scans both internally and from other hospitals, using the agreed procedures.7. Ensures accurate input of patient details when entering data onto information databases and the patient administration system (Careflow).8. Routinely uses the case note tracking system to ensure all patient case notes are tracked to their location.9. Support the Day Unit with the preparation of clinics.10. Provides cover in times of absence.11. Assists in ensuring timely delivery of notes to the appropriate department for out-patient appointments and in-patient admissions.12. Assists in the registration of new patients to ensure they are seen within the cancer waiting time targets.13. Exchange information with patients and staff on the admission and discharge of patients, both verbally and in written format.14. Communicate with patients who may be anxious, angry or upset.15. Exchange relevant information with GPs and other health professionals.16. Deal compassionately with distressing situations.17. Liaise with other members of staff regarding case notes and patient visits.18. Maintain patient confidentiality at all times.19. Always Remain professional when communicating with people in various situations.20. Undertakes other general office procedures, such as ordering stationery, opening and dispatching post, photocopying, printing etc.21. Any other duties deemed necessary for the effective running of the services, and in accordance with the grade of this post.22. Contributes to the training of new members of staff within a given area as required.23. Work with the Assistant Operations Manager and Secretaries to improve quality and range of services, with resources being managed according to agreed policies and priorities.24. To provide cross cover in periods of absence within the Administration Team and the wider Central Services Directorate
Person Specification
Qualifications
Essential
- Secondary-level education GCSW Maths and English at C-grade or above, or equivalent
- RSA/OCR typing/text transcription Stage II or equivalent experience
Desirable
- AMSPAR Full Diploma equivalent qualification
Experience
Essential
- Previous clerical and /or secretarial experience
- Experience of working with IT office packages
Desirable
- Previous clerical and/or secretarial experience in a hospital environment
- Experience of hospital administration system (PAS or equivalent)
Skills
Essential
- Audio / copy typing
- Word-processing - ability to produce accurate, well-presented work
- Excellent oral and written communication skills
- The ability to manage workload and priorities competing tasks effectively
Knowledge
Essential
- Knowledge and familiarity with a range of software including Word, Excel, database packages, e-mail and web browsers
Values
Essential
- Ability to work under pressure
- Ability to work as part of a team
- Able to use own initiative
- Reliability & confidentiality
- Ability to be flexible
Other
Essential
- To be flexible in order to meet the needs of the service and wider Central Services directorate
Person Specification
Qualifications
Essential
- Secondary-level education GCSW Maths and English at C-grade or above, or equivalent
- RSA/OCR typing/text transcription Stage II or equivalent experience
Desirable
- AMSPAR Full Diploma equivalent qualification
Experience
Essential
- Previous clerical and /or secretarial experience
- Experience of working with IT office packages
Desirable
- Previous clerical and/or secretarial experience in a hospital environment
- Experience of hospital administration system (PAS or equivalent)
Skills
Essential
- Audio / copy typing
- Word-processing - ability to produce accurate, well-presented work
- Excellent oral and written communication skills
- The ability to manage workload and priorities competing tasks effectively
Knowledge
Essential
- Knowledge and familiarity with a range of software including Word, Excel, database packages, e-mail and web browsers
Values
Essential
- Ability to work under pressure
- Ability to work as part of a team
- Able to use own initiative
- Reliability & confidentiality
- Ability to be flexible
Other
Essential
- To be flexible in order to meet the needs of the service and wider Central Services directorate
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Central Administration - E00040
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Central Administration - E00040
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
ACP Teenage and Young Adult (Haematology & Oncology)
The Christie NHS FT View all jobs
Posted 25 day(s) ago
Reference: 413-107839-CNS-LM-A
Job summary
An incredible opportunity has arisen to become part of our specialist Haematology and Transplant team at The Christie, delivering cutting-edge care to patients with haematological cancers. As home to the largest Teenage and Young Adult (TYA) Principal Treatment Centre in the North, we provide innovative, compassionate care to over 350 young people across inpatient, outpatient, and ambulatory settings.As a valued member of our forward-thinking and dedicated TYA team, you'll be at the forefront of shaping the cancer journey for young people, before, during, and beyond treatment. We actively encourage curiosity, professional growth, and innovation, empowering you to explore every dimension of TYA cancer care while making a lasting impact on patient experience and outcomes.We are seeking a passionate, highly motivated Advanced Clinical Practitioner (ACP) who is driven to deliver exceptional care and continuously improve services. You will bring substantial experience in medical and/or oncology settings, alongside an MSc in Advanced Clinical Practice.The post holder will work across the inpatient, outpatient and ambulatory setting as required. The role may in the future incorporate Weekends and Bank Holidays working.
Main duties of the job
o Provide clinical assessment and support to the care and treatment of a diverse caseload of patients requiring oncology/haematology input and transplant.o Demonstrate a highly specialist knowledge and skills in the diagnosis and management of patients with oncological/haematological malignancies and those requiring transplant.o Demonstrate a high level of specialist knowledge and skills in the acute care and management of patients receiving SACT.o Provide medical support to the inpatient, day unit and ambulatory care units at The Christie Foundation Trust.o Request investigations, procedures and make appropriate referrals maintaining relevant clinical records.o Non-Medical prescribing is fundamental in supporting this role.o Clinical examination skills are essential for this role.o Provide clinical expertise for developing and enhancing the TYA oncology, haematology and transplant service.o Work alongside the medical, AHP and nursing teams, maintaining good communication and collaboration between the various multidisciplinary teams.o To be a highly visible and approachable role model, ensuring that best practice is disseminated throughout the clinical areas.o Demonstrate a high commitment to the four pillars of Advanced Clinical Practice which includes Clinical practice, Education, Leadership and Management, and Research.
About us
The Christie is one of Europe's leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country. We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years.The Christie TYA & haematology service acts as a tertiary referral centre for the management of patients with oncology, haematological malignancies and bone marrow failure. Inpatient haematology and transplant services for both adults and Teenage and Young Adult (TYA) patients are provided by the 31 bedded Palatine Treatment Ward, and the 4 bedded Withington Ward. Outpatient TYA oncology/ haematology services are provided by the TYA Day Unit, Haematology and Transplant Day Unit (HTDU) and the ambulatory care facility. The Christie TYA & haematology service has grown extensively over the past few years with the development of new treatments and CAR T.
Details
Date posted
07 September 2026
Pay scheme
Agenda for change
Band
Band 8a
Salary
£57,528 to £64,750 a year Pro rata Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-107839-CNS-LM-A
Job locations
Haematology Oncology - E00292
The Christie NHS Foundation Trust Wilmslow Road
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
Along with the service line senior leadership team, including Advanced Practitioners and Consultant Practitioners, Advanced Practitioners will provide positive leadership, connecting patients, staff and partners with the vision and values of The Christie NHS Foundation Trust.They will use their expert knowledge and skills to assist in leading and delivering safe and clinically effective, quality driven, personalised care for people within our communities. Working alongside the senior managers and clinicians, they will assist in leading services that meet the needs of patients and their families to achieve improved health outcomes and promote health and wellbeing while demonstrating care, compassion, competence, communication, courage, and commitment.
The post holder will provide advanced and specialist level comprehensive assessments for patients with highly complex presentations, case management, treatment, and education. This will predominantly be delivered within the setting of their service line and may extend into inpatient and clinic settings to support with highly complex cases and patient pathways.
Central to the role will be critical thinking and using advanced decision-making skills to assess and manage patients accurately and safely. However, at no times should clinical staff work outside their defined level of competence. If the post holder has concerns regarding this, they should immediately discuss this with their line manager.
The Advanced Practitioners position is service driven and will cover the four pillars of advanced practice as outlined in the multi-professional framework for Advanced Practice in England (2025); clinical practice; leadership and management; education and training; research, quality improvement and service development.
The Advanced Practitioners role will support senior leadership collectively delivering high quality, effective and consistent care. Fostering effective working relationships with colleagues across a range of specialties and agencies.Provide clinical/professional supervision and support for clinical staff and trainee advanced practitioners within the service line not purely within their own profession. This will be in an associate workplace supervisor role once more than 2 years qualified and at 3 years can be as a coordinating education supervisor (as guided by the specific University) having attended a supervisor training course.
Provide education and development in the delivery of core and specialist training for the service line. The post holder will be expected to support in the creation of an environment of continuous quality improvement, develop clinical practice and care pathways designed around the people within our services and to ensure that delivery of care is regularly reviewed ensuring CQC compliance and embedding NICE and other quality benchmarks in good practice.
Assist in the maintenance of a culture of service improvement which promotes quality and safety and striving to improve and develop.
To support in embedding evidence-based practice, clinical research, supporting a research portfolio for studies within the service line, linking with relevant stakeholders and recruiting patients for studies in fields relevant to their clinical practice.To promote and support patient and public involvement in research. To assist in and undertake local and national audits. To identify and support implementation of service improvement plans. A job plan will be agreed to meet service and role needs, specifying the ratio of contracted hours to be spent delivering direct patients care (maximum 80%) and the time to be spent undertaking supported professional activity (minimum 20%), being reviewed annually or more frequently as required.
Please see attached Job Description for full list of role requirements and duties.
Job description
Job responsibilities
Along with the service line senior leadership team, including Advanced Practitioners and Consultant Practitioners, Advanced Practitioners will provide positive leadership, connecting patients, staff and partners with the vision and values of The Christie NHS Foundation Trust.They will use their expert knowledge and skills to assist in leading and delivering safe and clinically effective, quality driven, personalised care for people within our communities. Working alongside the senior managers and clinicians, they will assist in leading services that meet the needs of patients and their families to achieve improved health outcomes and promote health and wellbeing while demonstrating care, compassion, competence, communication, courage, and commitment.
The post holder will provide advanced and specialist level comprehensive assessments for patients with highly complex presentations, case management, treatment, and education. This will predominantly be delivered within the setting of their service line and may extend into inpatient and clinic settings to support with highly complex cases and patient pathways.
Central to the role will be critical thinking and using advanced decision-making skills to assess and manage patients accurately and safely. However, at no times should clinical staff work outside their defined level of competence. If the post holder has concerns regarding this, they should immediately discuss this with their line manager.
The Advanced Practitioners position is service driven and will cover the four pillars of advanced practice as outlined in the multi-professional framework for Advanced Practice in England (2025); clinical practice; leadership and management; education and training; research, quality improvement and service development.
The Advanced Practitioners role will support senior leadership collectively delivering high quality, effective and consistent care. Fostering effective working relationships with colleagues across a range of specialties and agencies.Provide clinical/professional supervision and support for clinical staff and trainee advanced practitioners within the service line not purely within their own profession. This will be in an associate workplace supervisor role once more than 2 years qualified and at 3 years can be as a coordinating education supervisor (as guided by the specific University) having attended a supervisor training course.
Provide education and development in the delivery of core and specialist training for the service line. The post holder will be expected to support in the creation of an environment of continuous quality improvement, develop clinical practice and care pathways designed around the people within our services and to ensure that delivery of care is regularly reviewed ensuring CQC compliance and embedding NICE and other quality benchmarks in good practice.
Assist in the maintenance of a culture of service improvement which promotes quality and safety and striving to improve and develop.
To support in embedding evidence-based practice, clinical research, supporting a research portfolio for studies within the service line, linking with relevant stakeholders and recruiting patients for studies in fields relevant to their clinical practice.To promote and support patient and public involvement in research. To assist in and undertake local and national audits. To identify and support implementation of service improvement plans. A job plan will be agreed to meet service and role needs, specifying the ratio of contracted hours to be spent delivering direct patients care (maximum 80%) and the time to be spent undertaking supported professional activity (minimum 20%), being reviewed annually or more frequently as required.
Please see attached Job Description for full list of role requirements and duties.
Person Specification
Qualifications
Essential
- Registered professional, (e.g., NMC/HCPC)
- Educated to MSc Degree Level 7 in advanced practice or equivalent, with NHSE Digital Staff badge demonstrating AP accreditation with The Centre for Advancing Practice
- IRM(E)R trained (where relevant to professional background and role)
- Blood product prescriber (where relevant to professional background and role)
- Non-medical prescriber (where relevant to professional background and role)
Desirable
- Teaching and assessing qualification
- Relevant research qualification - e.g., Good Clinical Practice
- Recognized leadership and management course
- Completion of relevant extended role scope competencies
Experience
Essential
- Experience of a senior professional role in relevant clinical specialty
- Enhanced clinical skills relevant to area of clinical practice
- Experienced in managing own caseload of patients as an independent practitioner
- Experience of implementing evidence-based practice
- Experience of working in partnership with multi-disciplinary teams
- Experience in undertaking audit, quality improvement and service evaluation
Desirable
- Experience of teaching and supervising undergraduate students and registered staff
- Experience of teaching and presenting at conference or other external meeting
- Experience of analysis and reporting of data
- Clinical experience of leading health care services within specialty
- Experience of research and implementation of evidence-based practice in relevant clinical specialty
- Experience in undertaking research projects and publishing articles
- Experience of inter-agency working and system delivery
Skills
Essential
- Excellent communication skills, written and verbal, to enable communication with a wide range of stakeholders and for clinical purposes, negotiation, leadership, and influence. This includes managing highly complex communications where there may be barriers to understanding
- Highly developed interpersonal skills, with meticulous attention to detail
- Complex planning and organisational skills
- Evidence of autonomous decision making
- Evidence of problem-solving skills
- Evidence of practice innovation and quality improvement
- IT skills for data management, reporting, presentation, and communication
- Evidence of enhanced clinical skills
- Self-motivated and able to prioritise within a large and varied workload
- Ability to identify and optimise learning opportunities
- Ability to work as part of a team and ability to command respect of the multi-disciplinary team
- Self-motivated, self-starter, and organised
- Flexible and adaptable at work to meet competing priorities
- Able to respond and prioritise unpredictable health presentations and ensure effective interventions are actioned
- Able to work in unpleasant working conditions on occasions, i.e., bodily fluids
- Enhanced knowledge of the multi-professional framework for advanced clinical practice (2025
Knowledge
Essential
- Enhanced knowledge relevant to the specialty area
- Knowledge of Quality Improvement methodologies and experience of successful delivery in practice
- Knowledge of leadership strategies, personal leadership and how to lead successful change in an organisation
- Knowledge of teaching and learning styles
- Safeguarding children and vulnerable adults
- Advanced knowledge of government strategies and policies relating to service and clinical leadership role
- Working knowledge of safety and governance frameworks and standards (including confidentiality/freedom of information/Caldicott regulations/CQC essential standards)
- Working knowledge of nursing, AHP and medical professional issues and developments
Values
Essential
- Ability to demonstrate the organisational values and behaviours of The Christie NHS Foundation Trust
Person Specification
Qualifications
Essential
- Registered professional, (e.g., NMC/HCPC)
- Educated to MSc Degree Level 7 in advanced practice or equivalent, with NHSE Digital Staff badge demonstrating AP accreditation with The Centre for Advancing Practice
- IRM(E)R trained (where relevant to professional background and role)
- Blood product prescriber (where relevant to professional background and role)
- Non-medical prescriber (where relevant to professional background and role)
Desirable
- Teaching and assessing qualification
- Relevant research qualification - e.g., Good Clinical Practice
- Recognized leadership and management course
- Completion of relevant extended role scope competencies
Experience
Essential
- Experience of a senior professional role in relevant clinical specialty
- Enhanced clinical skills relevant to area of clinical practice
- Experienced in managing own caseload of patients as an independent practitioner
- Experience of implementing evidence-based practice
- Experience of working in partnership with multi-disciplinary teams
- Experience in undertaking audit, quality improvement and service evaluation
Desirable
- Experience of teaching and supervising undergraduate students and registered staff
- Experience of teaching and presenting at conference or other external meeting
- Experience of analysis and reporting of data
- Clinical experience of leading health care services within specialty
- Experience of research and implementation of evidence-based practice in relevant clinical specialty
- Experience in undertaking research projects and publishing articles
- Experience of inter-agency working and system delivery
Skills
Essential
- Excellent communication skills, written and verbal, to enable communication with a wide range of stakeholders and for clinical purposes, negotiation, leadership, and influence. This includes managing highly complex communications where there may be barriers to understanding
- Highly developed interpersonal skills, with meticulous attention to detail
- Complex planning and organisational skills
- Evidence of autonomous decision making
- Evidence of problem-solving skills
- Evidence of practice innovation and quality improvement
- IT skills for data management, reporting, presentation, and communication
- Evidence of enhanced clinical skills
- Self-motivated and able to prioritise within a large and varied workload
- Ability to identify and optimise learning opportunities
- Ability to work as part of a team and ability to command respect of the multi-disciplinary team
- Self-motivated, self-starter, and organised
- Flexible and adaptable at work to meet competing priorities
- Able to respond and prioritise unpredictable health presentations and ensure effective interventions are actioned
- Able to work in unpleasant working conditions on occasions, i.e., bodily fluids
- Enhanced knowledge of the multi-professional framework for advanced clinical practice (2025
Knowledge
Essential
- Enhanced knowledge relevant to the specialty area
- Knowledge of Quality Improvement methodologies and experience of successful delivery in practice
- Knowledge of leadership strategies, personal leadership and how to lead successful change in an organisation
- Knowledge of teaching and learning styles
- Safeguarding children and vulnerable adults
- Advanced knowledge of government strategies and policies relating to service and clinical leadership role
- Working knowledge of safety and governance frameworks and standards (including confidentiality/freedom of information/Caldicott regulations/CQC essential standards)
- Working knowledge of nursing, AHP and medical professional issues and developments
Values
Essential
- Ability to demonstrate the organisational values and behaviours of The Christie NHS Foundation Trust
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Haematology Oncology - E00292
The Christie NHS Foundation Trust Wilmslow Road
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Haematology Oncology - E00292
The Christie NHS Foundation Trust Wilmslow Road
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
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Your application has been submitted.
Posted 25 day(s) ago
Reference: 413-109743-CNS-LM
Job summary
Join our collaborative SACT Outreach and Bloods Closer to Home team, supporting satellite sites across Greater Manchester and Cheshire. This rewarding role offers the opportunity to provide safe, effective, and person-centred care to patients in community settings, working alongside the Outreach team while also managing your own workload independently.You will work within multiple MDTs, developing strong communication skills and enhancing core clinical competencies, including phlebotomy and cannulation, through hands-on experience within blood rooms and Outreach facilities. As a key member of the team, you will support registered professionals, promote patient independence and wellbeing, and often be the reassuring face patients meet during their treatment journey.We are looking for someone who is compassionate, reliable, organised, and adaptable, with excellent communication skills and a commitment to learning and developing new clinical skills. The ability to respond confidently to changing service needs is essential.The role includes lone working and travel across Greater Manchester. Applicants must hold a full UK driving licence and have access to a vehicle. Mileage expenses are reimbursed in line with Trust policy.
Main duties of the job
Key Responsibilitieso Provide holistic, person-centred care to patients in the community and onsite.o Perform core clinical tasks within your competence, including phlebotomy (full training will be provided).o Follow Aseptic Non-Touch Technique (ANTT) and local infection prevention policies to maintain patient safety.o Work closely with registered nurses and other members of the multidisciplinary team.o Accurately record and report observations, interventions, and outcomes.o You will have the opportunity to work onsite (running outpatient clinics, working in our phlebotomy room as well as working in our bloods closer to home sites)o Skills & knowledge you will obtain if successful at interview are (not limited to): NEWS2, venepuncture, CVADS, TVADS, Height & weights, AKI & sepsis, urinalysis, ECG's, moving and handling, BLS & blood sugar monitoring.o Manage your workload effectively while working independently in the community.
Please see further information about our bloods closer to home service here: Bloods closer to homeIf you're compassionate, motivated and have a keen interest in becoming a Healthcare Assistant specialising in oncology and want to take the next step in your career, we'd love to hear from you.If you are interested, please contact SACT & Outpatients Lead nurse Gemma Jones [email protected]
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
07 September 2026
Pay scheme
Agenda for change
Band
Band 3
Salary
£25,760 to £27,476 a year Pro rata Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-109743-CNS-LM
Job locations
Outreach - E00010
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
1. Assists with the care of patients by:- Under the delegation of the Registered Nurse undertake care delivery, record the patient interventions carried out utilising the patients nursing records. These records must be countersigned by the Registered Nurse who delegated the duties.- Demonstrate respect for the individual patient, ensuring religious, cultural and social needs are considered at all times and acknowledge their individual rights.- Where required, assist nursing staff if they are conducting procedures or investigations.- Assisting patients in gaining access to, and in the use of, appropriate toilet facilities including catheter care, measuring and recording body waste/fluid balance accurately.- Ensure patients nutritional needs are met by assisting in the preparation of patients prior to meals and beverages, giving help and assistance in feeding/drinking as necessary. Record intake on food charts, where in place. Support nutritional monitoring by weighing patients.- Assist, direct and escort patients/visitors where and when appropriate.- Ensuring a clean and safe environment for patients and escalating any concerns.- Fluid balance monitoring.- Handling patients personal possessions, ensuring money and valuables are kept securely.- Providing enhanced therapeutic observations of care as required.- Carrying out of cardio-pulmonary resuscitation as required.
2. Complete all appropriate documentation relevant to care provided and update patients named nurse / shift coordinator where required.
3. Assist patients in maintaining their personal hygiene, grooming and dressing needs with specific concern for their religious, cultural and personal preference, ensuring privacy and dignity at all times.
4. Perform and record patients vital signs as directed - temperature, blood pressure, respiration and pulse, oxygen saturations, modified early warning scores, height & weight, urine testing (including Midstream Specimen, 24Hr urine collection, etc.) - as per Trust policy, reporting results to the Registered Nurse on duty, or in their absence to a Medic.
5. Provide a clinical phlebotomy service demonstrating expertise according to Phlebotomy guidelines and ensure that the samples and specimens are forwarded to appropriate laboratory services. Perform venous cannulation. Carry out central venous catheter bloods and central line care as per trust policy. Have a basic understanding of normal and altered blood values and escalate results as appropriate to the Registered Nurse or in their absence a Medic.
6. Perform electrocardiograms (ECG) in line with Trust policy and reporting to the Registered Nurse and/or medical staff once completed.
7. Prepare individual patients and the environment to ensure effective movement and/or handling procedures. Assist patients in their mobility requirements; provide assistance to patients moving from stretchers, wheelchairs and toilets. Assist patients to improve and maximise their mobility, utilising equipment as directed by the multi professional team.
8. Assist in meal service as required in line with Trust hygiene and food handling policy.
9. At the delegation of the Registered Nurse transfer the patient/client from one care area to another, i.e. outpatients environment to discharge lounge/ward/other department. Chaperone the patient as required ensuring appropriate support.
10. Welcome and orientate patients, visitors and others to the unit/department and ensure that all communications result in effective customer care.
11. Assist in the correct procedure of duties relating to last offices for deceased persons. Ensure that all religious and cultural wishes, obligations are adhered with, in line with Trust policies and procedures..
12. Communicate well within the team at all times. Demonstrate a pleasant and approachable manner and help create and promote a good team working relationship, by being fully involved, committed and participative to achieving full potential. Proactively help patients and carers to take an active role in care delivery. Develop personal awareness of others perceptions, acknowledging and changing behaviour in response to any constructive feedback.
13. If working under bloods closer to home, you must own and hold vehicle business insurance, must hold valid UK drivers license and be confident driving around Greater Manchester and surrounding areas
14. Must feel confident and comfortable working alone and travelling around our satellite bloods closer to home sites delivering pre treatment investigations i.e. venepuncture and ECGs
Clinical Support:
1. Where appropriate, to answer queries promptly and courteously, taking appropriate actions according to the mode of enquiry or the information required. As appropriate, inform or refer enquiries or problems to the relevant qualified staff.
2. Assist the Registered Nurse in the process of undertaking clinical risk assessments e.g. recording height and weight, updating the nurse on any changes to a patients condition/ circumstances. Responsibility for undertaking the risk assessments lies with the Registered Nurse.
3. Appropriately record and monitor dietary intake of patients, informing relevant staff of progress and/or any difficulties relating to dietary/fluid intake.
4. Assist in providing conditions to meet the patients need for rest and sleep.
5. Actively support and assist in alleviating distress and anxiety of patients or carers, consistent with their personal beliefs and preferences.
6. Prepare trolleys for specific clinical procedures in line with trust policy utilising asceptic non touch technique practices.
7. Recognise and report abusive behaviour to an appropriate member of staff, documenting the same.
Environmental Support:
1. Be responsible for self and others through identifying risks and undertaking work activities in a safe manner.
2. Maintain cleanliness in the work environment, ensuring a clean and safe environment for patients, adhering to infection control policies and guidance in line with Trust health and safety policies.
3. Prepare and maintain environments for clinical procedures.
4. Contribute to the general tidiness and cleanliness of the clinical environment including the correct disposal of waste.
5. Assist with the checking of clinic/department linen stock, where required. Contribute to the supply and maintenance of materials and equipment to ensure the efficient running of the clinical environment.
6. Assist with the checking and recording of deliveries to the clinical areas against original orders. Ensure stock rotation is undertaken to minimise the risk of equipment becoming out of date.
7. Assist in the transfer of materials and equipment as requested, including the maintenance of equipment as appropriate.
8. Report faults on the clinic/unit/department as necessary.
9. Reports all accidents and complaints according to the agreed policy to shift coordinator or senior staff.
10. Contributes to the continuous improvement of services. May be required to demonstrate and assist more junior staff to gain clinical experience, skills and knowledge.
11. Undertake all training required to perform duties effectively to the requirements of the post, including but not limited to attending all required mandatory training courses.
12. Maintain own professional portfolio in accordance with personal development plans.
13. Demonstrates the agreed set of values and accountable for own attitude and behaviour.
Administration:
1. Assist in preparing patients notes, relevant charts, nursing documentation, etc. and ensure that patient notes are available within the clinic/department and secure at all times.
2. Undertake clerical duties as directed by the Registered Nurse in relation to all verbal and written communications, ensuring messages and communications are passed to other team members, storage of patient information and retrieval of such information.
These duties and responsibilities are neither exclusive nor exhaustive and staff may be required to undertake other duties and responsibilities consistent with the band.
Job description
Job responsibilities
1. Assists with the care of patients by:- Under the delegation of the Registered Nurse undertake care delivery, record the patient interventions carried out utilising the patients nursing records. These records must be countersigned by the Registered Nurse who delegated the duties.- Demonstrate respect for the individual patient, ensuring religious, cultural and social needs are considered at all times and acknowledge their individual rights.- Where required, assist nursing staff if they are conducting procedures or investigations.- Assisting patients in gaining access to, and in the use of, appropriate toilet facilities including catheter care, measuring and recording body waste/fluid balance accurately.- Ensure patients nutritional needs are met by assisting in the preparation of patients prior to meals and beverages, giving help and assistance in feeding/drinking as necessary. Record intake on food charts, where in place. Support nutritional monitoring by weighing patients.- Assist, direct and escort patients/visitors where and when appropriate.- Ensuring a clean and safe environment for patients and escalating any concerns.- Fluid balance monitoring.- Handling patients personal possessions, ensuring money and valuables are kept securely.- Providing enhanced therapeutic observations of care as required.- Carrying out of cardio-pulmonary resuscitation as required.
2. Complete all appropriate documentation relevant to care provided and update patients named nurse / shift coordinator where required.
3. Assist patients in maintaining their personal hygiene, grooming and dressing needs with specific concern for their religious, cultural and personal preference, ensuring privacy and dignity at all times.
4. Perform and record patients vital signs as directed - temperature, blood pressure, respiration and pulse, oxygen saturations, modified early warning scores, height & weight, urine testing (including Midstream Specimen, 24Hr urine collection, etc.) - as per Trust policy, reporting results to the Registered Nurse on duty, or in their absence to a Medic.
5. Provide a clinical phlebotomy service demonstrating expertise according to Phlebotomy guidelines and ensure that the samples and specimens are forwarded to appropriate laboratory services. Perform venous cannulation. Carry out central venous catheter bloods and central line care as per trust policy. Have a basic understanding of normal and altered blood values and escalate results as appropriate to the Registered Nurse or in their absence a Medic.
6. Perform electrocardiograms (ECG) in line with Trust policy and reporting to the Registered Nurse and/or medical staff once completed.
7. Prepare individual patients and the environment to ensure effective movement and/or handling procedures. Assist patients in their mobility requirements; provide assistance to patients moving from stretchers, wheelchairs and toilets. Assist patients to improve and maximise their mobility, utilising equipment as directed by the multi professional team.
8. Assist in meal service as required in line with Trust hygiene and food handling policy.
9. At the delegation of the Registered Nurse transfer the patient/client from one care area to another, i.e. outpatients environment to discharge lounge/ward/other department. Chaperone the patient as required ensuring appropriate support.
10. Welcome and orientate patients, visitors and others to the unit/department and ensure that all communications result in effective customer care.
11. Assist in the correct procedure of duties relating to last offices for deceased persons. Ensure that all religious and cultural wishes, obligations are adhered with, in line with Trust policies and procedures..
12. Communicate well within the team at all times. Demonstrate a pleasant and approachable manner and help create and promote a good team working relationship, by being fully involved, committed and participative to achieving full potential. Proactively help patients and carers to take an active role in care delivery. Develop personal awareness of others perceptions, acknowledging and changing behaviour in response to any constructive feedback.
13. If working under bloods closer to home, you must own and hold vehicle business insurance, must hold valid UK drivers license and be confident driving around Greater Manchester and surrounding areas
14. Must feel confident and comfortable working alone and travelling around our satellite bloods closer to home sites delivering pre treatment investigations i.e. venepuncture and ECGs
Clinical Support:
1. Where appropriate, to answer queries promptly and courteously, taking appropriate actions according to the mode of enquiry or the information required. As appropriate, inform or refer enquiries or problems to the relevant qualified staff.
2. Assist the Registered Nurse in the process of undertaking clinical risk assessments e.g. recording height and weight, updating the nurse on any changes to a patients condition/ circumstances. Responsibility for undertaking the risk assessments lies with the Registered Nurse.
3. Appropriately record and monitor dietary intake of patients, informing relevant staff of progress and/or any difficulties relating to dietary/fluid intake.
4. Assist in providing conditions to meet the patients need for rest and sleep.
5. Actively support and assist in alleviating distress and anxiety of patients or carers, consistent with their personal beliefs and preferences.
6. Prepare trolleys for specific clinical procedures in line with trust policy utilising asceptic non touch technique practices.
7. Recognise and report abusive behaviour to an appropriate member of staff, documenting the same.
Environmental Support:
1. Be responsible for self and others through identifying risks and undertaking work activities in a safe manner.
2. Maintain cleanliness in the work environment, ensuring a clean and safe environment for patients, adhering to infection control policies and guidance in line with Trust health and safety policies.
3. Prepare and maintain environments for clinical procedures.
4. Contribute to the general tidiness and cleanliness of the clinical environment including the correct disposal of waste.
5. Assist with the checking of clinic/department linen stock, where required. Contribute to the supply and maintenance of materials and equipment to ensure the efficient running of the clinical environment.
6. Assist with the checking and recording of deliveries to the clinical areas against original orders. Ensure stock rotation is undertaken to minimise the risk of equipment becoming out of date.
7. Assist in the transfer of materials and equipment as requested, including the maintenance of equipment as appropriate.
8. Report faults on the clinic/unit/department as necessary.
9. Reports all accidents and complaints according to the agreed policy to shift coordinator or senior staff.
10. Contributes to the continuous improvement of services. May be required to demonstrate and assist more junior staff to gain clinical experience, skills and knowledge.
11. Undertake all training required to perform duties effectively to the requirements of the post, including but not limited to attending all required mandatory training courses.
12. Maintain own professional portfolio in accordance with personal development plans.
13. Demonstrates the agreed set of values and accountable for own attitude and behaviour.
Administration:
1. Assist in preparing patients notes, relevant charts, nursing documentation, etc. and ensure that patient notes are available within the clinic/department and secure at all times.
2. Undertake clerical duties as directed by the Registered Nurse in relation to all verbal and written communications, ensuring messages and communications are passed to other team members, storage of patient information and retrieval of such information.
These duties and responsibilities are neither exclusive nor exhaustive and staff may be required to undertake other duties and responsibilities consistent with the band.
Person Specification
Qualifications
Essential
- Vocational healthcare qualification at Level 3 or equivalent experience.
- Basic Literacy and Numeracy skills.
Desirable
- Speciality specific training.
Experience
Essential
- Experience of working in a healthcare environment, undertaking a range of clinical commitments.
- Experience of working with a multi-disciplinary team.
Desirable
- Experience of working within more than one speciality within a health care environment.
- Oncology experience.
Sk
Essential
- Good communication skills (written and verbal).
- Competent in clinical skills appropriate to the job role (including taking and recording vital signs, ECGs, phlebotomy, cannulation).
- Basic IT skills.
- Must hold a full UK drivers license and own an operational vehicle.
Desirable
- Ability to demonstrate care skills to more junior healthcare support workers.
Knowledge
Essential
- In-depth understanding of the healthcare support worker role in an outpatient setting.
- Participate in personal development.
Desirable
- Evidence of recent training.
Values
Essential
- Ability to demonstrate the organisational values and behaviours.
Personal Attributes
Essential
- Committed to delivering high standards of patient/customer care.
- Empathetic and Caring.
- Professional outlook and positive attitude.
- Honest and trustworthy.
- Able to meet the flexible needs of the role and duty roster (including weekend working where required).
Person Specification
Qualifications
Essential
- Vocational healthcare qualification at Level 3 or equivalent experience.
- Basic Literacy and Numeracy skills.
Desirable
- Speciality specific training.
Experience
Essential
- Experience of working in a healthcare environment, undertaking a range of clinical commitments.
- Experience of working with a multi-disciplinary team.
Desirable
- Experience of working within more than one speciality within a health care environment.
- Oncology experience.
Sk
Essential
- Good communication skills (written and verbal).
- Competent in clinical skills appropriate to the job role (including taking and recording vital signs, ECGs, phlebotomy, cannulation).
- Basic IT skills.
- Must hold a full UK drivers license and own an operational vehicle.
Desirable
- Ability to demonstrate care skills to more junior healthcare support workers.
Knowledge
Essential
- In-depth understanding of the healthcare support worker role in an outpatient setting.
- Participate in personal development.
Desirable
- Evidence of recent training.
Values
Essential
- Ability to demonstrate the organisational values and behaviours.
Personal Attributes
Essential
- Committed to delivering high standards of patient/customer care.
- Empathetic and Caring.
- Professional outlook and positive attitude.
- Honest and trustworthy.
- Able to meet the flexible needs of the role and duty roster (including weekend working where required).
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Outreach - E00010
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Outreach - E00010
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Specialist Clinical Pharmacist - Clinical Haematology
The Christie NHS FT View all jobs
Posted 1 month(s) ago
Reference: 413-109377-CSSS-RS-A
Job summary
We are one of the largest oncology Trusts in the UK with an international reputation for clinical excellence, research and development. As part of a collaborative venture between The Christie NHS Trust and MCHFT to develop clinical haematology services, the Christie is pleased to be able to offer an exciting opportunity for a specialist clinical pharmacist to join the clinical haematology team This is a unique opportunity to work with us at a new peripheral centre based on the Mid Cheshire Hospitals site and contribute to the challenging and rewarding specialty of haemato-oncology pharmacy, delivering advanced clinical care to patients with haematological cancers and general haematological conditions.
We are integral members of the MDT, and we are expanding our roles in existing services such out-patient clinics and peripheral site services, which the post-holder will develop alongside the Lead Pharmacists. We are also developing links with the University of Manchester and working on collaborative projects at the main site, with scope to role this out further at peripheral sites.The postholder must possess an independent prescribing qualification to assist in the MDT outpatient clinics. They will play a key role in the future development of outpatient services within the highly regarded haematology MDT, implementing new initiatives in collaboration with the Lead Haematology Pharmacist and Lead Pharmacist for Clinical Services.
Main duties of the job
To provide a highly specialist clinical pharmacy services to outpatients within the Christie Haematology @ Leighton Service and develop a good working partnership with internal and external stakeholders to ensure a high quality SACT service is provided to patients.
The specialist pharmacist will work across the clinical haematology outpatient service at Leighton Hospital alongside a team of clinical haematology consultants, advanced nurse practitioner and clinical nurse specialists.
Pharmacist independent prescribing responsibilities support this practice. The specialist clinical pharmacist is expected to contribute to planning, education, research, and participate in clinical audit within own area of practice.To deliver and evaluate clinical pharmacy services to both malignant and non-malignant haematology patients in conjunction with the Lead Haematology Pharmacist and Clinical Haematology service manager.To support the multidisciplinary team in the safe, efficient and cost-effective use of medicine resources to the designated cancer disease group by the provision of education and training, procedures, policies and guidelines, and medicine usage information.Although the outpatient service is based at Mid Cheshire Hospitals NHS Foundation Trust site , postholders may be required to work at any location across the Greater Manchester and Cheshire Cancer Network.
About us
The Christie is one of Europe's leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country. We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years. We run one of the largest early clinical trial units in Europe with over 300 trials every year. Cancer research in Manchester, most of which is undertaken on the Christie site, has been officially ranked the best in the UK.This is a unique opportunity to work with us and contribute to the challenging and rewarding specialty of haemato-oncology pharmacy.
Details
Date posted
03 September 2026
Pay scheme
Agenda for change
Band
Band 8a
Salary
£57,528 to £64,750 a year Pro rata, per annum
Contract
Fixed term
Duration
12 months
Working pattern
Full-time
Reference number
413-109377-CSSS-RS-A
Job locations
Pharmacy Clinical - E00920
Leighton Hospital, Middlewich Road
Crewe
CW1 4QJ
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
To provide a highly specialist clinical pharmacy services to outpatients within the Christie Haematology @ Leighton Service and develop a good working partnership with internal and external stakeholders to ensure a high quality SACT service is provided to patients.. To provide specialist clinical pharmacy services to haematology patients with both malignant and non-malignant conditions in accordance with all departmental, Trust national and international standards, procedures and policies. To be responsible for the delivery and development of an out-patient clinical practice,
Provides expert professional advice to patients/clients, carers, and staff, working in partnerships with patients, families, and other professionals to formulate robust care pathways that are ethically sound and in the interest of the patients.
To be an independent prescriber and prescribe to appropriate patients in agreement with the relevant consultants.
Maintain and develop expertise and competence within the field of clinical haematology to enable collaboration with other practitioners and medical staff, and to facilitate the management of patients.
To consent patients for treatment and procedures as per hospital policy if deemed appropriate within scope of competency and practice.
Communicate complex, sensitive, or contentious information to patients and carers. This may include results of scans; management options and discusses details of prognosis including palliative care if deemed appropriate within scope of competency and practice.
Educate patients and their carers on issues surrounding health promotion and illness prevention. Promote and facilitate changes to lifestyle where appropriate.
To work closely with and provide pharmaceutical advice to medical staff, other members of the multi-disciplinary team and patients.
To contribute to the development, of and maintenance of the peripheral site pharmacy provision on the Christie Haematology @ Leighton Service unit in conjunction with The Mid Cheshire NHS trust pharmacy services and the Christie Trust NHS and third-party providers responsible for supplying supportive care medication and SACT including clinical trial medications, where appropriate.
To work with the peripheral site clinical trials pharmacist, where appropriate on development of site initiation on existing trials and other trial related activities, as required To provide a highly specialised clinical pharmacy service. Ensure patient centered care and that the use of medicines is optimised. This will include:
Taking drug histories on admission/ completion of medicines reconciliation Review of medication to ensure its safe and effective use Review of medication in line with interpretation of appropriate results of investigations Therapeutic drug monitoring as appropriate Patient education about their medicines Participation in Multidisciplinary team meetings Development of evidence-based treatment protocols for use within individual departments or Trust wide Facilitate the implementation of local and national guidelines Influencing prescribers, encourage formulary compliance where appropriate. Demonstrating professional accountability to patients
To conduct appropriate drug use reviews within oncology as determined by the Medicines Management Group or individual departments.
To assist consultants within the Christie Haematology @ Leighton Service in the preparation of new drug requests/ unlicensed drug applications for submission to the drug and therapeutics committee
To monitor the Christie Haeamtology @ Leighton drug expenditure regarding haematology services assessing any financial pressures. Identify changes in prescribing practice that may impact on the setting of the drugs budget, including new prescribing practice (horizon scanning) and report to Director of pharmacy, Lead Haematology pharmacists and Clinical Haematology Service Manager
To attend relevant MDT meetings, relevant specialist pharmacy groups and contribute to meetings relevant to the designated disease group as appropriate.
To communicate with general practitioners and community pharmacists regarding the supply of unusual or non-standard medicines.
To participate in service evaluation and future initiatives, audit, record clinical interventions and activity data.
Contributes to the education program to all health care professionals in informal and formal settings relating to haematology practice. This will be training and education locally, nationally, and internationally (e.g., presenting at meetings, study days, conferences).
Acts as a role model, educator, supervisor, coach, and mentor, seeking to instil and develop the confidence of others To undertake clinical audit and practice research as part of the multi-disciplinary audit process within the designated disease group and clinical pharmacy service.
To support, develop and maintain drug protocols, treatment guidelines and standard operating procedures both within the clinical pharmacy service and the haematology unit. Reviewing evidence-based guidelines and protocols in conjunction with fellow healthcare professionals, in order to advance the safe, clinical effective and cost-efficient use of medicines for patients.
To be aware of the processes surrounding the maintenance of local and national databases surrounding medication use related to the haematology service including immunoglobulins.
To ensure compliance with the Trust patient safety schemes.
To ensure appropriate use of antibiotics and antifungal agents and contribute to relevant audits as required.. Represent the haematology service at appropriate clinical unit and divisional meetings including peripheral site MDT group meetings on request.
To monitor and interpret published evidence and computer reports of drug usage, to use this data to report to the lead clinicians and Director of Pharmacy, implementing agreed policies aimed at improving patient outcomes and containing drug expenditure.
To support the Electronic Prescribing process across the Trust.
To support the designated cancer disease group through the development and implementation of electronic prescribing for outpatients.
To support prescribing at the individual patient level, contributing to the optimisation of patients drug therapy with due consideration to risk/benefit issues.
Facilitate effective communication about relevant pharmacy issues to clinicians and senior managers and the identification of opportunities for development of pharmacy services to match identified services and care needs.
To demonstrate awareness and commitment to the Trusts Clinical Governance Plan.
In conjunction with the Lead Haematology Pharmacist and Principal Pharmacist in Clinical Services, to establish processes for the setting of standards of care, identifying the risks involved and implement changes that need to occur to achieve these.
To identify and report any systemic or preventable errors associated with medicines within the Cancer Centre Services Division and facilitate learning.
General Duties
To assist and participate in the development, implementation and management of training initiatives and competency frameworks
Together with colleagues to be involved in the maintenance of cost-effective and efficient pharmacy services and to participate in their regular review and development.
To represent pharmacy and act as a link person at relevant meetings and conferences.
To provide education and training to pharmacy, medical and nursing staff. To participate in the clinical training of pharmacists and foundation year trainee pharmacists if required.
To be responsible for the clinical screening/review of SACT prescriptions for designated patient groups, including clinical trial prescriptions and to clinically screen/ review in-patient and outpatient prescriptions.
To give advice on the storage, administration and therapeutic use of drugs to patients, medical / nursing staff and other colleagues. To provide written information as necessary.
To follow local, Trust and National guidelines for safe medicines practice.
To identify own training needs and maintain a CPD portfolio. To undertake any other duties consistent with the nature of the post as requested by the Pharmacy Managers and the Trust.
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
To provide a highly specialist clinical pharmacy services to outpatients within the Christie Haematology @ Leighton Service and develop a good working partnership with internal and external stakeholders to ensure a high quality SACT service is provided to patients.. To provide specialist clinical pharmacy services to haematology patients with both malignant and non-malignant conditions in accordance with all departmental, Trust national and international standards, procedures and policies. To be responsible for the delivery and development of an out-patient clinical practice,
Provides expert professional advice to patients/clients, carers, and staff, working in partnerships with patients, families, and other professionals to formulate robust care pathways that are ethically sound and in the interest of the patients.
To be an independent prescriber and prescribe to appropriate patients in agreement with the relevant consultants.
Maintain and develop expertise and competence within the field of clinical haematology to enable collaboration with other practitioners and medical staff, and to facilitate the management of patients.
To consent patients for treatment and procedures as per hospital policy if deemed appropriate within scope of competency and practice.
Communicate complex, sensitive, or contentious information to patients and carers. This may include results of scans; management options and discusses details of prognosis including palliative care if deemed appropriate within scope of competency and practice.
Educate patients and their carers on issues surrounding health promotion and illness prevention. Promote and facilitate changes to lifestyle where appropriate.
To work closely with and provide pharmaceutical advice to medical staff, other members of the multi-disciplinary team and patients.
To contribute to the development, of and maintenance of the peripheral site pharmacy provision on the Christie Haematology @ Leighton Service unit in conjunction with The Mid Cheshire NHS trust pharmacy services and the Christie Trust NHS and third-party providers responsible for supplying supportive care medication and SACT including clinical trial medications, where appropriate.
To work with the peripheral site clinical trials pharmacist, where appropriate on development of site initiation on existing trials and other trial related activities, as required To provide a highly specialised clinical pharmacy service. Ensure patient centered care and that the use of medicines is optimised. This will include:
Taking drug histories on admission/ completion of medicines reconciliation Review of medication to ensure its safe and effective use Review of medication in line with interpretation of appropriate results of investigations Therapeutic drug monitoring as appropriate Patient education about their medicines Participation in Multidisciplinary team meetings Development of evidence-based treatment protocols for use within individual departments or Trust wide Facilitate the implementation of local and national guidelines Influencing prescribers, encourage formulary compliance where appropriate. Demonstrating professional accountability to patients
To conduct appropriate drug use reviews within oncology as determined by the Medicines Management Group or individual departments.
To assist consultants within the Christie Haematology @ Leighton Service in the preparation of new drug requests/ unlicensed drug applications for submission to the drug and therapeutics committee
To monitor the Christie Haeamtology @ Leighton drug expenditure regarding haematology services assessing any financial pressures. Identify changes in prescribing practice that may impact on the setting of the drugs budget, including new prescribing practice (horizon scanning) and report to Director of pharmacy, Lead Haematology pharmacists and Clinical Haematology Service Manager
To attend relevant MDT meetings, relevant specialist pharmacy groups and contribute to meetings relevant to the designated disease group as appropriate.
To communicate with general practitioners and community pharmacists regarding the supply of unusual or non-standard medicines.
To participate in service evaluation and future initiatives, audit, record clinical interventions and activity data.
Contributes to the education program to all health care professionals in informal and formal settings relating to haematology practice. This will be training and education locally, nationally, and internationally (e.g., presenting at meetings, study days, conferences).
Acts as a role model, educator, supervisor, coach, and mentor, seeking to instil and develop the confidence of others To undertake clinical audit and practice research as part of the multi-disciplinary audit process within the designated disease group and clinical pharmacy service.
To support, develop and maintain drug protocols, treatment guidelines and standard operating procedures both within the clinical pharmacy service and the haematology unit. Reviewing evidence-based guidelines and protocols in conjunction with fellow healthcare professionals, in order to advance the safe, clinical effective and cost-efficient use of medicines for patients.
To be aware of the processes surrounding the maintenance of local and national databases surrounding medication use related to the haematology service including immunoglobulins.
To ensure compliance with the Trust patient safety schemes.
To ensure appropriate use of antibiotics and antifungal agents and contribute to relevant audits as required.. Represent the haematology service at appropriate clinical unit and divisional meetings including peripheral site MDT group meetings on request.
To monitor and interpret published evidence and computer reports of drug usage, to use this data to report to the lead clinicians and Director of Pharmacy, implementing agreed policies aimed at improving patient outcomes and containing drug expenditure.
To support the Electronic Prescribing process across the Trust.
To support the designated cancer disease group through the development and implementation of electronic prescribing for outpatients.
To support prescribing at the individual patient level, contributing to the optimisation of patients drug therapy with due consideration to risk/benefit issues.
Facilitate effective communication about relevant pharmacy issues to clinicians and senior managers and the identification of opportunities for development of pharmacy services to match identified services and care needs.
To demonstrate awareness and commitment to the Trusts Clinical Governance Plan.
In conjunction with the Lead Haematology Pharmacist and Principal Pharmacist in Clinical Services, to establish processes for the setting of standards of care, identifying the risks involved and implement changes that need to occur to achieve these.
To identify and report any systemic or preventable errors associated with medicines within the Cancer Centre Services Division and facilitate learning.
General Duties
To assist and participate in the development, implementation and management of training initiatives and competency frameworks
Together with colleagues to be involved in the maintenance of cost-effective and efficient pharmacy services and to participate in their regular review and development.
To represent pharmacy and act as a link person at relevant meetings and conferences.
To provide education and training to pharmacy, medical and nursing staff. To participate in the clinical training of pharmacists and foundation year trainee pharmacists if required.
To be responsible for the clinical screening/review of SACT prescriptions for designated patient groups, including clinical trial prescriptions and to clinically screen/ review in-patient and outpatient prescriptions.
To give advice on the storage, administration and therapeutic use of drugs to patients, medical / nursing staff and other colleagues. To provide written information as necessary.
To follow local, Trust and National guidelines for safe medicines practice.
To identify own training needs and maintain a CPD portfolio. To undertake any other duties consistent with the nature of the post as requested by the Pharmacy Managers and the Trust.
Person Specification
Qualifications
Essential
- Vocational Masters Degree or equivalent in Pharmacy
- Membership of General Pharmaceutical Council
- Post Graduate Diploma in Clinical Pharmacy or equivalent
- Evidence of continuing professional development
- Independent prescribing qualification
Desirable
- Advanced communication skills
Experience
Essential
- Relevant post registration hospital pharmacy experience within oncology and/or haemato-oncology
- Financial awareness and drug budgets
- Providing medicines information and advice
- Screening/ reviewing prescriptions including oral chemotherapy.
- Training or teaching pharmacy/nursing/medical staff
- Experience of multidisciplinary team working
Desirable
- Audit or research work.
Skills
Essential
- Teaching and presentation skills and have excellent interpersonal and communication skills for conveying complex concepts.
- Ability to coach, motivate and inspire
- Networking amongst internal and external professional/organisation
- Able to work efficiently and use own initiative and have good time management
- Work within and always promote the Trusts values and behaviours
Desirable
- Project implementation.
Knowledge
Essential
- Evidence of a sound clinical knowledge base in clinical hematology and haemato oncology.
- Knowledge of clinical governance
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Quality clinical governance and risk assessment abilities
- Patient and customer focus
- Continuous Improvement
Desirable
- Demonstrates clinical governance
Person Specification
Qualifications
Essential
- Vocational Masters Degree or equivalent in Pharmacy
- Membership of General Pharmaceutical Council
- Post Graduate Diploma in Clinical Pharmacy or equivalent
- Evidence of continuing professional development
- Independent prescribing qualification
Desirable
- Advanced communication skills
Experience
Essential
- Relevant post registration hospital pharmacy experience within oncology and/or haemato-oncology
- Financial awareness and drug budgets
- Providing medicines information and advice
- Screening/ reviewing prescriptions including oral chemotherapy.
- Training or teaching pharmacy/nursing/medical staff
- Experience of multidisciplinary team working
Desirable
- Audit or research work.
Skills
Essential
- Teaching and presentation skills and have excellent interpersonal and communication skills for conveying complex concepts.
- Ability to coach, motivate and inspire
- Networking amongst internal and external professional/organisation
- Able to work efficiently and use own initiative and have good time management
- Work within and always promote the Trusts values and behaviours
Desirable
- Project implementation.
Knowledge
Essential
- Evidence of a sound clinical knowledge base in clinical hematology and haemato oncology.
- Knowledge of clinical governance
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Quality clinical governance and risk assessment abilities
- Patient and customer focus
- Continuous Improvement
Desirable
- Demonstrates clinical governance
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Pharmacy Clinical - E00920
Leighton Hospital, Middlewich Road
Crewe
CW1 4QJ
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Pharmacy Clinical - E00920
Leighton Hospital, Middlewich Road
Crewe
CW1 4QJ
United Kingdom
Employer's website
Apply Now
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Posted 1 month(s) ago
Reference: 413-104518-CSSS-SD-A
Job summary
Acute Assessment Unit
Band 5 Registered Nurse
34.5 - permanent
The AAU is recruiting!
Due to service developments, we are seeking experienced nurses to join our team.
Oncology experience is not essential as acute care skills are more relevant to this area however an interest in oncology nursing is desired.
We care for all emergency/unplanned admissions to The Christie, dealing with a variety of general medical problems, alongside acute complications of cancer treatment.
There are many benefits to working on The Christie Acute Assessment Unit:
Newly built unit with spacious clinical areas for efficient working & patient and staff experience
Standard nurse: patient ratio of 1:4/6
8 weeks induction period to help you learn the role and get to know the ward
Good training and development opportunitiesOncology and palliative care specific study days in supernumerary periodWard based clinical practice facilitator to aid development and learning
Many staff benefits/discounts available
On-going support from a friendly team of Ward Sisters
Acute Medicine Consultants based on the ward
An opportunity to develop your acute care and oncology skills
For further information, please contact:
Sophia McGough - [email protected]
Matron
Main duties of the job
To provide care for patients who are admitted to the unit as an emergency and their carers within a recognised framework in accordance with NMC Code of Professional Conduct, Christie NHS Trust policies and Health & Safety legislation.
About us
The Christie is one of Europe's leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country. We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years. We run one of the largest early clinical trial units in Europe with over 300 trials every year. Cancer research in Manchester, most of which is undertaken on the Christie site, has been officially ranked the best in the UK.
Details
Date posted
03 September 2026
Pay scheme
Agenda for change
Band
Band 5
Salary
£32,073 to £39,043 a year per annum pro rata
Contract
Permanent
Working pattern
Full-time
Reference number
413-104518-CSSS-SD-A
Job locations
Acute Assessment Unit - E00851
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
Professional
.Manage and generally supervise the ward in the absence of senior staff.
Take individual responsibility for the nursing care of a group of patients as a registered nurse
3. Provide a supportive role within the Acute Assessment Unit for nursing, medical and clerical Staff
4. Undertake the nursing care of patients, ensuring privacy & dignity is maintained whilst being aware of physical and psychological needs
5. To give a clear and accurate update at change of duties and ensure accurate documentation of nursing interventions
6. To participate in the emergency care of patients and give any necessary instructions, including transfer information
7. Participate in nursing procedures appropriate to the department
8. Support and assist in the induction/training of junior staff/Health Care Assistants acting as mentor to designated staff
9. To welcome patients to the ward and its routine
10. Be able to act as ward co-ordinator and ensure the safe and timely through put of patients, liaising closely with triage/admission staff, medical staff and other wards
11. To liaise with medical and para medical personnel and community organisations
12. To highlight areas of improvement/development within the department and undertake relevant projects
13. To act as support for other ward nurses in relation to acute emergency care
14. Safely escort patients to other areas and collect blood products from key departments
15. Assist in the provision of meals / refreshments for patients whilst meeting their nutritional needs
16. Assist in the general housekeeping duties of the AAU
17. Help to maintain a safe environment and report faults/risks etc to the nurse in charge
18. Liaise with staff member responsible for stores/stationery and ordering and assist in the maintenance of stock levels
19. Handles patients personal possessions, ensure cash and valuables kept securely as per policy
20. Correct care and custody of controlled drugs and aid the safe storage of medicines
21. Assist medical staff with procedures
22. Carry out certain procedures such as cannulation and 12 lead ECGs and be prepared to learn new skills
EDUCATIONAL DEVELOPMENT
1. The staff nurse is responsible for their own personal development and maintaining a personal development plan
2. To complete the Ward introductory pack and preceptor pack
3. Complete Principles and Practice of Intravenous Skills Programme and Cannulation Skills Training and update annually
4. Annually attend all mandatory study days as per Trust and unit guidance
PERSONAL
1. Demonstrate a pleasant and approachable manner and help create and promote a good working relationship
2. Show professional and courteous manner when answering the telephone and other enquires
3. Maintain confidentiality with regard to patient information both at work and outside of working hours
4. To be aware of and adhere to all policies including; sickness and absence, confidentiality, uniform and responsibilities under the Health and Safety at work act and be familiar with all risk assessments pertinent to the AAU
5. Report and record all accidents and complaints according to the agreed policy
6. To be aware of limitations and utilise the preceptor system for any issues that arise
7. To show respect for members of the team and endorse the AAUs philosophy of giving mutual support
8. Demonstrates the agreed set of values and accountable for own attitude and behaviour
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
Professional
.Manage and generally supervise the ward in the absence of senior staff.
Take individual responsibility for the nursing care of a group of patients as a registered nurse
3. Provide a supportive role within the Acute Assessment Unit for nursing, medical and clerical Staff
4. Undertake the nursing care of patients, ensuring privacy & dignity is maintained whilst being aware of physical and psychological needs
5. To give a clear and accurate update at change of duties and ensure accurate documentation of nursing interventions
6. To participate in the emergency care of patients and give any necessary instructions, including transfer information
7. Participate in nursing procedures appropriate to the department
8. Support and assist in the induction/training of junior staff/Health Care Assistants acting as mentor to designated staff
9. To welcome patients to the ward and its routine
10. Be able to act as ward co-ordinator and ensure the safe and timely through put of patients, liaising closely with triage/admission staff, medical staff and other wards
11. To liaise with medical and para medical personnel and community organisations
12. To highlight areas of improvement/development within the department and undertake relevant projects
13. To act as support for other ward nurses in relation to acute emergency care
14. Safely escort patients to other areas and collect blood products from key departments
15. Assist in the provision of meals / refreshments for patients whilst meeting their nutritional needs
16. Assist in the general housekeeping duties of the AAU
17. Help to maintain a safe environment and report faults/risks etc to the nurse in charge
18. Liaise with staff member responsible for stores/stationery and ordering and assist in the maintenance of stock levels
19. Handles patients personal possessions, ensure cash and valuables kept securely as per policy
20. Correct care and custody of controlled drugs and aid the safe storage of medicines
21. Assist medical staff with procedures
22. Carry out certain procedures such as cannulation and 12 lead ECGs and be prepared to learn new skills
EDUCATIONAL DEVELOPMENT
1. The staff nurse is responsible for their own personal development and maintaining a personal development plan
2. To complete the Ward introductory pack and preceptor pack
3. Complete Principles and Practice of Intravenous Skills Programme and Cannulation Skills Training and update annually
4. Annually attend all mandatory study days as per Trust and unit guidance
PERSONAL
1. Demonstrate a pleasant and approachable manner and help create and promote a good working relationship
2. Show professional and courteous manner when answering the telephone and other enquires
3. Maintain confidentiality with regard to patient information both at work and outside of working hours
4. To be aware of and adhere to all policies including; sickness and absence, confidentiality, uniform and responsibilities under the Health and Safety at work act and be familiar with all risk assessments pertinent to the AAU
5. Report and record all accidents and complaints according to the agreed policy
6. To be aware of limitations and utilise the preceptor system for any issues that arise
7. To show respect for members of the team and endorse the AAUs philosophy of giving mutual support
8. Demonstrates the agreed set of values and accountable for own attitude and behaviour
Person Specification
Qualifications
Essential
- RGN Level 1 or 2
- Degree or Diploma in Nursing
Desirable
- Post Graduate certificate in cancer care / oncology or acute care
- Post graduate certificate in teaching and assessing
Experience
Essential
- Experience in an acute care/oncology setting
Desirable
- Post Reg acute care/oncology experience
Skills
Essential
- Good communication skills
- Ability to deliver high standard of nursing care
- Computer literacy
- Understanding need for evidence based practice
Desirable
- Cannulation/venepuncture skills
- ECG'S
Knowledge
Essential
- Participate in personal development
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Desirable
- Understanding/experience of current national initiatives
Other
Essential
- Rotation to night duty as required
- Team player
- Willingness to be involved with ward/unit/Trust initiatives
Desirable
- Understanding/experience of current national initiatives
Person Specification
Qualifications
Essential
- RGN Level 1 or 2
- Degree or Diploma in Nursing
Desirable
- Post Graduate certificate in cancer care / oncology or acute care
- Post graduate certificate in teaching and assessing
Experience
Essential
- Experience in an acute care/oncology setting
Desirable
- Post Reg acute care/oncology experience
Skills
Essential
- Good communication skills
- Ability to deliver high standard of nursing care
- Computer literacy
- Understanding need for evidence based practice
Desirable
- Cannulation/venepuncture skills
- ECG'S
Knowledge
Essential
- Participate in personal development
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Desirable
- Understanding/experience of current national initiatives
Other
Essential
- Rotation to night duty as required
- Team player
- Willingness to be involved with ward/unit/Trust initiatives
Desirable
- Understanding/experience of current national initiatives
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Acute Assessment Unit - E00851
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Acute Assessment Unit - E00851
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-110314-EF-DA
Job summary
We are seeking a motivated and aspiring Senior Supervisor to join the supervisory team within the Estate and Facilities Division, Site Services Directorate.
Working closely with Deputy Support Service Managers, the post holder will provide guidance and support to Domestic Supervisors in the day-to-day management of services, promoting positive staff performance, attendance and wellbeing, and fostering an inclusive and supportive working environment. The role is responsible for overseeing Domestic Supervisors, Domestic Assistants, Deep Clean Assistants and the pest control service, ensuring all services are delivered consistently, effectively and in compliance with NHS Cleaning Standards, legal and statutory standards.
We are committed to investing in our people, and training and development opportunities will be provided to support the successful candidate in developing their leadership skills and reaching their full potential.
Based at our main site in Withington, this Band 4 position offers 37.5 hours per week, 27 days annual leave plus bank holidays, rising with length of service, and membership of the NHS Pension Scheme. Elements of the service operate 24 hours a day, 7 days a week, and working hours will vary in line with service needs, with appropriate notice given of any roster changes.
If you are looking for the next step in your career and want to develop as a leader within a world-renowned organisation, this could be the opportunity for you.
Main duties of the job
As our Senior Supervisor, you will be responsible for the effective delivery and oversight of:o Cleaning services across clinical and non-clinical areaso Deep cleaning services, Discharge cleaning serviceo Infection Prevention and Control through targeted cleaning activitieso Staff wellbeing, including welfare meetings, Occupational Health referrals and risk assessmentso Staff Rotas, Service compliance, systems and procedureso Environmental walkabouts to monitor standards and drive improvements
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
03 September 2026
Pay scheme
Agenda for change
Band
Band 4
Salary
£28,392 to £31,157 a year Pro Rata, Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-110314-EF-DA
Job locations
Domestics - E00235
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
1. Operational Service Delivery
Support the delivery of domestic and deep clean services in line with service specifications, Trust procedures and the National Standards of Healthcare Cleanliness. Ensure adequate staffing levels are maintained to deliver high quality services, including reactive and emergency cleaning responses. Coordinate daily work allocation, cleaning schedules and rotas to ensure continuity and consistency of service delivery. Participate in and support rapid response and emergency cleaning requirements as required. Ensure services are delivered efficiently, making effective use of resources while maintaining safety and quality standards.
2. Leadership, Supervision and Staff SupportProvide day to day supervision, guidance and support to domestic and deep clean staff, and support Domestic Supervisors in the effective management of their teams. Promote positive performance, attendance, conduct and wellbeing in line with Trust policies and the NHS People Promise. Support staff induction, training, ongoing development and refresher training to ensure competence, compliance and service continuity. Support the training of clinical teams in relation to cleaning responsibilities, in line with the National Standards of Healthcare Cleanliness. Conduct return to work discussions and attendance support processes, including phased returns, risk assessments, Occupational Health referrals and staff wellbeing initiatives, liaising with the Deputy Support Services Manager as appropriate. Arrange and conduct stages of the management of attendance process in accordance with Trust policy and procedures. Support recruitment activities using the Trusts e recruitment system (Trac), including shortlisting, coordination of interviews and onboarding processes, in line with Trust guidance. Undertake regular one to one meetings and development reviews with Domestic Supervisors and domestic/deep clean staff to support performance, development and engagement. Foster an inclusive, respectful and supportive working environment that values diversity, promotes equality and complies with Trust Equality and Diversity Policy.
3. Quality, Audit and Infection PreventionMonitor cleaning standards through routine audits, inspections and electronic monitoring systems, working in partnership with Infection Prevention and Control teams. Ensure timely follow up of audit actions and contribute to service improvements where standards fall below expected levels. Undertake regular ward and departmental visits to monitor quality, address concerns and provide operational support. Contribute to investigations and responses to complaints, incidents and feedback related to cleaning services, identifying learning opportunities and supporting continuous improvement.
4. Communication and Partnership WorkingAct as a point of contact for operational cleaning matters, responding to enquiries in a professional, courteous and timely manner. Communicate effectively with colleagues, patients, visitors and stakeholders to support service delivery and maintain positive working relationships. Work collaboratively with clinical and non clinical teams to support cleaning requirements and service developments. Hold service meetings, toolbox talks and staff briefings to ensure clear communication, engagement and awareness.
5. Training, Competence and DevelopmentDeliver or support operational training, including the safe use of cleaning equipment, products and approved cleaning procedures. Provide guidance and advice to staff to support safe working practices, health and safety compliance and service quality. Maintain own knowledge, skills and mandatory training requirements, including the effective use of IT and electronic monitoring systems relevant to the role.
6. Health, Safety and Risk ManagementEnsure staff work in compliance with health and safety legislation, COSHH requirements and local risk assessments. Support the reporting, investigation and follow up of incidents and near misses using Trust reporting systems. Promote a culture of safety and take appropriate action to address unsafe practices or environments, escalating concerns where required.
7. Resources and Stock ControlSupport the management of stock control, ordering and distribution of cleaning consumables and equipment. Ensure equipment is used correctly, maintained appropriately and reported promptly for repair or servicing as required. Contribute to the accurate completion and maintenance of departmental records, including rotas, stock usage and operational documentation.
8. Operational DecisionMaking and EscalationWork within Trust and departmental policies, procedures and guidelines, using initiative to resolve routine operational issues. Escalate complex, sensitive or high risk issues to the Deputy Support Services Manager as appropriate.
9. Work Environment and DemandsThe role requires regular movement across clinical and nonclinical areas of the Trust. The post holder may occasionally work in demanding environments, including checking or supporting cleaning in patient care areas requiring enhanced infection prevention measures, and in areas with higher levels of dust or pest issues, supported by appropriate training and controls. Physical activity may include demonstrating cleaning techniques, operating cleaning equipment and handling supplies. The role involves managing competing priorities and responding to interruptions within a busy operational environment.
Job description
Job responsibilities
1. Operational Service Delivery
Support the delivery of domestic and deep clean services in line with service specifications, Trust procedures and the National Standards of Healthcare Cleanliness. Ensure adequate staffing levels are maintained to deliver high quality services, including reactive and emergency cleaning responses. Coordinate daily work allocation, cleaning schedules and rotas to ensure continuity and consistency of service delivery. Participate in and support rapid response and emergency cleaning requirements as required. Ensure services are delivered efficiently, making effective use of resources while maintaining safety and quality standards.
2. Leadership, Supervision and Staff SupportProvide day to day supervision, guidance and support to domestic and deep clean staff, and support Domestic Supervisors in the effective management of their teams. Promote positive performance, attendance, conduct and wellbeing in line with Trust policies and the NHS People Promise. Support staff induction, training, ongoing development and refresher training to ensure competence, compliance and service continuity. Support the training of clinical teams in relation to cleaning responsibilities, in line with the National Standards of Healthcare Cleanliness. Conduct return to work discussions and attendance support processes, including phased returns, risk assessments, Occupational Health referrals and staff wellbeing initiatives, liaising with the Deputy Support Services Manager as appropriate. Arrange and conduct stages of the management of attendance process in accordance with Trust policy and procedures. Support recruitment activities using the Trusts e recruitment system (Trac), including shortlisting, coordination of interviews and onboarding processes, in line with Trust guidance. Undertake regular one to one meetings and development reviews with Domestic Supervisors and domestic/deep clean staff to support performance, development and engagement. Foster an inclusive, respectful and supportive working environment that values diversity, promotes equality and complies with Trust Equality and Diversity Policy.
3. Quality, Audit and Infection PreventionMonitor cleaning standards through routine audits, inspections and electronic monitoring systems, working in partnership with Infection Prevention and Control teams. Ensure timely follow up of audit actions and contribute to service improvements where standards fall below expected levels. Undertake regular ward and departmental visits to monitor quality, address concerns and provide operational support. Contribute to investigations and responses to complaints, incidents and feedback related to cleaning services, identifying learning opportunities and supporting continuous improvement.
4. Communication and Partnership WorkingAct as a point of contact for operational cleaning matters, responding to enquiries in a professional, courteous and timely manner. Communicate effectively with colleagues, patients, visitors and stakeholders to support service delivery and maintain positive working relationships. Work collaboratively with clinical and non clinical teams to support cleaning requirements and service developments. Hold service meetings, toolbox talks and staff briefings to ensure clear communication, engagement and awareness.
5. Training, Competence and DevelopmentDeliver or support operational training, including the safe use of cleaning equipment, products and approved cleaning procedures. Provide guidance and advice to staff to support safe working practices, health and safety compliance and service quality. Maintain own knowledge, skills and mandatory training requirements, including the effective use of IT and electronic monitoring systems relevant to the role.
6. Health, Safety and Risk ManagementEnsure staff work in compliance with health and safety legislation, COSHH requirements and local risk assessments. Support the reporting, investigation and follow up of incidents and near misses using Trust reporting systems. Promote a culture of safety and take appropriate action to address unsafe practices or environments, escalating concerns where required.
7. Resources and Stock ControlSupport the management of stock control, ordering and distribution of cleaning consumables and equipment. Ensure equipment is used correctly, maintained appropriately and reported promptly for repair or servicing as required. Contribute to the accurate completion and maintenance of departmental records, including rotas, stock usage and operational documentation.
8. Operational DecisionMaking and EscalationWork within Trust and departmental policies, procedures and guidelines, using initiative to resolve routine operational issues. Escalate complex, sensitive or high risk issues to the Deputy Support Services Manager as appropriate.
9. Work Environment and DemandsThe role requires regular movement across clinical and nonclinical areas of the Trust. The post holder may occasionally work in demanding environments, including checking or supporting cleaning in patient care areas requiring enhanced infection prevention measures, and in areas with higher levels of dust or pest issues, supported by appropriate training and controls. Physical activity may include demonstrating cleaning techniques, operating cleaning equipment and handling supplies. The role involves managing competing priorities and responding to interruptions within a busy operational environment.
Person Specification
Qualifications
Essential
- NVQ Level 4 (or equivalent) in Cleaning, Facilities, Supervision or Customer Services or equivalent demonstrable experience
- Functional Skills Level 2 / GCSE (or equivalent) in English
Desirable
- Willingness to work towards NVQ Level 5 or equivalent in cleaning and support services
Experience
Essential
- Experience working within cleaning, domestic, facilities or support services
- Experience of supervising staff, including rota allocation and service coordination
- Experience of maintaining service standards in a regulated or operational environment
- Experience managing attendance/wellbeing issues
Desirable
- Previous experience working within a healthcare or NHS environment
Skills
Essential
- Effective verbal and written communication skills
- Ability to manage routine performance or conduct issues in line with Trust policies
- Ability to remain calm in a busy environment
- Basic IT skills relevant to the role (e.g. email, e-rostering, monitoring systems)
Desirable
- Familiar with Synbiotix monitoring systems.
Knowledge
Essential
- Cleaning methods, equipment and safe systems of work
- Infection Prevention and Control principles
- Health & Safety and COSHH requirements
- Equality, Diversity and Inclusion principles
Desirable
- Awareness of National Standards of Healthcare Cleanliness
Values
Essential
- Professional, reliable and flexible approach to work
- Supportive and inclusive management style
- Commitment to patient-focused services and high standards
- Demonstrates Trust values and behaviours, including respect and inclusion
Desirable
- Evidence of champion diversity and inclusion
Others
Essential
- Must be able to work unsocial hours and demonstrate flexibility to meet service needs
Person Specification
Qualifications
Essential
- NVQ Level 4 (or equivalent) in Cleaning, Facilities, Supervision or Customer Services or equivalent demonstrable experience
- Functional Skills Level 2 / GCSE (or equivalent) in English
Desirable
- Willingness to work towards NVQ Level 5 or equivalent in cleaning and support services
Experience
Essential
- Experience working within cleaning, domestic, facilities or support services
- Experience of supervising staff, including rota allocation and service coordination
- Experience of maintaining service standards in a regulated or operational environment
- Experience managing attendance/wellbeing issues
Desirable
- Previous experience working within a healthcare or NHS environment
Skills
Essential
- Effective verbal and written communication skills
- Ability to manage routine performance or conduct issues in line with Trust policies
- Ability to remain calm in a busy environment
- Basic IT skills relevant to the role (e.g. email, e-rostering, monitoring systems)
Desirable
- Familiar with Synbiotix monitoring systems.
Knowledge
Essential
- Cleaning methods, equipment and safe systems of work
- Infection Prevention and Control principles
- Health & Safety and COSHH requirements
- Equality, Diversity and Inclusion principles
Desirable
- Awareness of National Standards of Healthcare Cleanliness
Values
Essential
- Professional, reliable and flexible approach to work
- Supportive and inclusive management style
- Commitment to patient-focused services and high standards
- Demonstrates Trust values and behaviours, including respect and inclusion
Desirable
- Evidence of champion diversity and inclusion
Others
Essential
- Must be able to work unsocial hours and demonstrate flexibility to meet service needs
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Domestics - E00235
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Domestics - E00235
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
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Posted 1 month(s) ago
Reference: 413-106551-CICE-LM
Job summary
The main purpose of the role is to support the Experimental Cancer Medicine Team with all aspects of clinical trials administration, according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and Trust policies. The post holder will provide support to the Senior Clinical Trials Coordinators and wider Clinical Research Team.The post holder will assist with the administration of clinical trials from feasibility to archiving including (but not limited to):
o Assist with the efficient and timely set up of clinical trials.o Assist with the tracking and raising of invoices.o Manage own workload for daily trial activity including case report form completion and amendment processing to meet internal and external deadlines.o Assist with quality assurance of all trial related documentation in accordance with relevant legislation and guidelines.o Assist with preparation for audit and inspections within assigned teams.o General trial-related communication in accordance with the Data Protection Act.
Main duties of the job
The specific responsibilities will depend on the requirements of each team, but may include:
o Act as a point of contact for the R&I core team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to trial set up and general trial conduct.o Set up and initiation of allocated trials within an assigned team, under the guidance of the Senior Clinical Trials Coordinators.o Track all payments throughout each clinical trial including completion of activity logs and requesting invoices to be raised.o Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready.o Process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines.o Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety reporting in accordance with protocol requirements.o Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature.o Arrange team and trial related meetings as required, producing minutes in a timely manner.o Ensure that data is available and up to date for any meetings related to a clinical trial.
PLEASE REFER TO THE JOB DESCRIPTION FOR A FULL LIST OF DUTIES.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
03 September 2026
Pay scheme
Agenda for change
Band
Band 4
Salary
£28,392 to £31,157 a year Pro rata Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-106551-CICE-LM
Job locations
Phase 1 - Q01312
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
The specific responsibilities will depend on the requirements of each team, but may include:
Act as a point of contact for the core Research and Development team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to trial set up and general trial conduct.
Set up and initiation of allocated trials within an assigned team, under the guidance of the Senior Clinical Trials Coordinators.
Track all payments throughout each clinical trial including completion of activity logs and requesting invoices to be raised.
Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times.
Process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines.
Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety reporting in accordance with protocol requirements.
Complete team reporting mechanisms (i.e. recruitment activity logs, patient visit logs, costing spreadsheets, case report form trackers and electronic proformas).
Produce trial workbooks for review by the lead Clinical Research Nurse and Principal Investigator for assigned studies and ensure version control is maintained.
Ensure collection of clinical case notes for all patients, so that these are available as needed, for monitoring and audit purposes.
Complete case report forms as per sponsor requirements, and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits.
Cross check, confirm data and complete query resolution with sponsors and third parties in a timely manner.
Completion of clinical trial specific databases with data from various sources such as questionnaires, hospital records and other electronic and paper sources.
Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature.
Arrange shipping and delivery of relevant trial data and documents including import/export of tumour blocks, ECGs and copy scans.
Arrange team and trial related meetings as required, producing minutes in a timely manner.
Ensure that data is available and up to date for any meetings related to a clinical trial.
If required attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team.
Assist with preparation for audit and inspections within assigned teams.
Assist with trial document archiving by following the Trusts archiving guidelines.
Ensure that office/ trial related supplies are adequate and assist with the ordering process.
Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment Teams.
Demonstrates the agreed set of values and accountable for own attitude and behaviour.
Job description
Job responsibilities
The specific responsibilities will depend on the requirements of each team, but may include:
Act as a point of contact for the core Research and Development team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to trial set up and general trial conduct.
Set up and initiation of allocated trials within an assigned team, under the guidance of the Senior Clinical Trials Coordinators.
Track all payments throughout each clinical trial including completion of activity logs and requesting invoices to be raised.
Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times.
Process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines.
Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety reporting in accordance with protocol requirements.
Complete team reporting mechanisms (i.e. recruitment activity logs, patient visit logs, costing spreadsheets, case report form trackers and electronic proformas).
Produce trial workbooks for review by the lead Clinical Research Nurse and Principal Investigator for assigned studies and ensure version control is maintained.
Ensure collection of clinical case notes for all patients, so that these are available as needed, for monitoring and audit purposes.
Complete case report forms as per sponsor requirements, and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits.
Cross check, confirm data and complete query resolution with sponsors and third parties in a timely manner.
Completion of clinical trial specific databases with data from various sources such as questionnaires, hospital records and other electronic and paper sources.
Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature.
Arrange shipping and delivery of relevant trial data and documents including import/export of tumour blocks, ECGs and copy scans.
Arrange team and trial related meetings as required, producing minutes in a timely manner.
Ensure that data is available and up to date for any meetings related to a clinical trial.
If required attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team.
Assist with preparation for audit and inspections within assigned teams.
Assist with trial document archiving by following the Trusts archiving guidelines.
Ensure that office/ trial related supplies are adequate and assist with the ordering process.
Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment Teams.
Demonstrates the agreed set of values and accountable for own attitude and behaviour.
Person Specification
Qualifications
Essential
- Diploma or Administration experience.
Desirable
- Degree in Science or Health related discipline.
- Relevant training courses in Clinical Research.
- Qualification in computing or information technology /Relevant IT experience.
Experience
Essential
- Experience in Administration including data management.
Desirable
- Experience of working within a Clinical Trials environment.
- Relevant experience within a Good Clinical Practice and Research Environment.
Skills
Essential
- Good written communication skills.
- Good understanding and demonstrated use of Microsoft Word and Excel.
- Accuracy and attention to detail.
- Good organisational skills.
- Good interpersonal skills.
- Good oral communication skills.
Desirable
- Good understanding and demonstrated use of the full Microsoft Office suite.
Knowledge
Essential
- Knowledge of the Clinical Trials process.
- Familiar with GCP guidelines/EU directives.
Desirable
- Understanding of Medical Terminology and Cancer.
- Understanding of case report forms.
- Knowledge of Clinical Governance.
- Knowledge of patient information systems.
Values
Essential
- Ability to demonstrate the organisational values and behaviours.
Other
Essential
- Ability to work to tight and/or unexpected deadlines.
- Flexible with ability to adapt to service requirements.
- Hardworking; ability to manage a busy workload.
- Ability to work unsupervised or as part of a team.
- Tactful and diplomatic.
Desirable
- Ability to troubleshoot effectively.
Person Specification
Qualifications
Essential
- Diploma or Administration experience.
Desirable
- Degree in Science or Health related discipline.
- Relevant training courses in Clinical Research.
- Qualification in computing or information technology /Relevant IT experience.
Experience
Essential
- Experience in Administration including data management.
Desirable
- Experience of working within a Clinical Trials environment.
- Relevant experience within a Good Clinical Practice and Research Environment.
Skills
Essential
- Good written communication skills.
- Good understanding and demonstrated use of Microsoft Word and Excel.
- Accuracy and attention to detail.
- Good organisational skills.
- Good interpersonal skills.
- Good oral communication skills.
Desirable
- Good understanding and demonstrated use of the full Microsoft Office suite.
Knowledge
Essential
- Knowledge of the Clinical Trials process.
- Familiar with GCP guidelines/EU directives.
Desirable
- Understanding of Medical Terminology and Cancer.
- Understanding of case report forms.
- Knowledge of Clinical Governance.
- Knowledge of patient information systems.
Values
Essential
- Ability to demonstrate the organisational values and behaviours.
Other
Essential
- Ability to work to tight and/or unexpected deadlines.
- Flexible with ability to adapt to service requirements.
- Hardworking; ability to manage a busy workload.
- Ability to work unsupervised or as part of a team.
- Tactful and diplomatic.
Desirable
- Ability to troubleshoot effectively.
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Phase 1 - Q01312
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Phase 1 - Q01312
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-107637-CSSS-LM-A
Job summary
Are you passionate about Patient Safety and Experience and wish to support staff to improve care? We are looking for an experienced registered healthcare professional to join the Divisional Clinical Governance Team.The post holder will have a patient centred approach and will work in such a way as to help promote an open and transparent culture that actively improves clinical safety and quality and seek to make improvements to enhance the patient experience and safety.You will support the clinical governance manager to manage and co-ordinate all aspects of patient safety, risk management and governance within the CSSS division, ensuring the effective application of the Trusts' Risk Management Strategy. You will be required to work closely with the ward managers, Matrons and Service Leads, supporting learning responses to incident investigation, complaints management, clinical audit and the development of policies and procedures to support safe, high-quality care.This is a fast-paced role, where priorities can change at very short notice, so we're looking for someone who can work well under pressure, manage competing priorities and work to deadlines.
Main duties of the job
The Assistant Clinical Governance Manager will work collaboratively across the Trust to support the Clinical Governance Manager to develop the Clinical Governance plans; to ensure that national, trust wide and divisional standards are delivered and monitored and that patient, staff and visitor safety is considered and improved where possible and that risks which may damage the reputation or have a financial impact on the Trust are mitigated to their lowest level.
About us
The Christie is one of Europe's leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country. We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years. We run one of the largest early clinical trial units in Europe with over 300 trials every year. Cancer research in Manchester, most of which is undertaken on the Christie site, has been officially ranked the best in the UK.
Details
Date posted
03 September 2026
Pay scheme
Agenda for change
Band
Band 6
Salary
£39,959 to £48,117 a year Pro rata Per Annum
Contract
Fixed term
Duration
6 months
Working pattern
Full-time
Reference number
413-107637-CSSS-LM-A
Job locations
Senior Nursing & Governance - E01005
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
Contribute to clinical governance policy development and implementation and the embedding of new and existing systems and processes across the division.
Promote a culture of risk management across the division.
Work collaboratively to monitor and achieve divisional objectives, in relation to clinical governance processes and policies.
In conjunction with the management teams within the division, provide staff with expert advice as necessary on risk management, practice, service evaluation and audit.
Support divisional managers with the implementation of the clinical governance agenda, including the risk management strategy and contribute to the Corporate Clinical Governance and Risk Strategies as required.
Collaborate with the Trusts Quality & Standards Team to ensure governance and risk management processes are integrated with, and congruent to, corporate strategy.
Evaluate current practice in the division through standard setting and audit, promoting evidence-based practice, ensuring clinical leaders and managers are involved.
Lead and support others to lead the appropriate levels of incident investigations in the division.
Influence and contribute to the development and delivery of training and development for all members of the multi-professional teams in the division to enhance patient care and monitor the implementation and evaluation of the divisions training strategy in relation to risk management.
Leadership
Support the clinical governance manager with leading the provision and development of a specialist level of risk management support to the division and manage, in conjunction with lead clinicians, the implementation of the risk management objectives within the division.
Motivate and inspire others to create and maintain enthusiasm for the clinical governance agenda and a good working environment. Actively seek to improve the services provided.
Support the integration of research evidence into practice.
Support the divisional clinical governance manager and senior management team in collaboration with professional heads of service and consultant leads for clinical governance, review national guidelines, reports and recommendations, ensuring local action plans are devised to meet national recommendations. Monitor the implementation of such action plans, producing exception reports for the divisional board where necessary.
System Monitoring and Report Production
Review incident forms and risk assessments and analyse, identify and report significant risk trends and issues arising at a ward, department, specialty or divisional level. This involves receiving, analysing and presenting highly complex and sensitive information relating to incidents and complaints involving patients, members of the public and healthcare staff.
Assist the clinical governance manager in the preparation and presentation of timely written and verbal reports pertaining to risk as required for a variety of audiences including the divisional board and the Trust risk & quality governance committee. This information must be clear and succinct and focus management action towards key areas of risk.
Provide practical guidance to managers and staff regarding the population and use of the risk register as a tool to support all Trust staff to monitor progress made against risks identified.
In conjunction with lead clinicians, maintain and evaluate the risk register within the division, monitoring implementation of agreed actions and updating the register following quarterly review, escalating relevant issues to the divisional board as appropriate.
Incident Investigation
Lead investigations and support other staff in the division to investigate significant incidents and near misses with the multi-disciplinary team to ensure that Trust-wide policy guiding investigations is followed and that action plans are developed, implemented, monitored, and reviewed for effectiveness. Ensure that outstanding actions are escalated using the Trust systems and processes and present these findings back to the divisional board, executive review group and relevant staff groups.
Promote the dissemination of recommendations from reviews. Support the division in learning from reviews and feedback lessons learnt across the Trust and externally where appropriate.
Assist the clinical governance manager to provide expert advice on existing and new legislation and guidance and specific advice in the event of serious untoward incidents (SUIs). Facilitate root cause analysis meetings and alike, to following serious incidents and monitor the implementation of any recommendations arising from investigations, disseminate Trust wide learning and report internally and externally as appropriate.
Work closely with the health and safety manager and support the resolution of non-clinical risk issues where appropriate.
Service Improvement / Practice Development
In collaboration with lead nurses and other professional heads identify areas where professional practice could be improved and lead change in collaboration with other professionals to improve care.
Working in collaboration with the divisional management team, respond to patient views and external assessment to identify areas of potential practice development.
Work directly with clinical staff as required ensuring that practice standards are being implemented.
Ensure current clinical guidance, external reviews and accreditations are discussed and reviewed by senior clinicians within agreed time limits, consultation takes place with staff and/or patient groups and changes are communicated to staff.
Education
Facilitate a supportive, learning environment for practitioners.
Assist in the production of learning bulletins/newsletters, ensuring content provides clinical updates for staff; production is timely, and content is quality controlled.
Job description
Job responsibilities
Contribute to clinical governance policy development and implementation and the embedding of new and existing systems and processes across the division.
Promote a culture of risk management across the division.
Work collaboratively to monitor and achieve divisional objectives, in relation to clinical governance processes and policies.
In conjunction with the management teams within the division, provide staff with expert advice as necessary on risk management, practice, service evaluation and audit.
Support divisional managers with the implementation of the clinical governance agenda, including the risk management strategy and contribute to the Corporate Clinical Governance and Risk Strategies as required.
Collaborate with the Trusts Quality & Standards Team to ensure governance and risk management processes are integrated with, and congruent to, corporate strategy.
Evaluate current practice in the division through standard setting and audit, promoting evidence-based practice, ensuring clinical leaders and managers are involved.
Lead and support others to lead the appropriate levels of incident investigations in the division.
Influence and contribute to the development and delivery of training and development for all members of the multi-professional teams in the division to enhance patient care and monitor the implementation and evaluation of the divisions training strategy in relation to risk management.
Leadership
Support the clinical governance manager with leading the provision and development of a specialist level of risk management support to the division and manage, in conjunction with lead clinicians, the implementation of the risk management objectives within the division.
Motivate and inspire others to create and maintain enthusiasm for the clinical governance agenda and a good working environment. Actively seek to improve the services provided.
Support the integration of research evidence into practice.
Support the divisional clinical governance manager and senior management team in collaboration with professional heads of service and consultant leads for clinical governance, review national guidelines, reports and recommendations, ensuring local action plans are devised to meet national recommendations. Monitor the implementation of such action plans, producing exception reports for the divisional board where necessary.
System Monitoring and Report Production
Review incident forms and risk assessments and analyse, identify and report significant risk trends and issues arising at a ward, department, specialty or divisional level. This involves receiving, analysing and presenting highly complex and sensitive information relating to incidents and complaints involving patients, members of the public and healthcare staff.
Assist the clinical governance manager in the preparation and presentation of timely written and verbal reports pertaining to risk as required for a variety of audiences including the divisional board and the Trust risk & quality governance committee. This information must be clear and succinct and focus management action towards key areas of risk.
Provide practical guidance to managers and staff regarding the population and use of the risk register as a tool to support all Trust staff to monitor progress made against risks identified.
In conjunction with lead clinicians, maintain and evaluate the risk register within the division, monitoring implementation of agreed actions and updating the register following quarterly review, escalating relevant issues to the divisional board as appropriate.
Incident Investigation
Lead investigations and support other staff in the division to investigate significant incidents and near misses with the multi-disciplinary team to ensure that Trust-wide policy guiding investigations is followed and that action plans are developed, implemented, monitored, and reviewed for effectiveness. Ensure that outstanding actions are escalated using the Trust systems and processes and present these findings back to the divisional board, executive review group and relevant staff groups.
Promote the dissemination of recommendations from reviews. Support the division in learning from reviews and feedback lessons learnt across the Trust and externally where appropriate.
Assist the clinical governance manager to provide expert advice on existing and new legislation and guidance and specific advice in the event of serious untoward incidents (SUIs). Facilitate root cause analysis meetings and alike, to following serious incidents and monitor the implementation of any recommendations arising from investigations, disseminate Trust wide learning and report internally and externally as appropriate.
Work closely with the health and safety manager and support the resolution of non-clinical risk issues where appropriate.
Service Improvement / Practice Development
In collaboration with lead nurses and other professional heads identify areas where professional practice could be improved and lead change in collaboration with other professionals to improve care.
Working in collaboration with the divisional management team, respond to patient views and external assessment to identify areas of potential practice development.
Work directly with clinical staff as required ensuring that practice standards are being implemented.
Ensure current clinical guidance, external reviews and accreditations are discussed and reviewed by senior clinicians within agreed time limits, consultation takes place with staff and/or patient groups and changes are communicated to staff.
Education
Facilitate a supportive, learning environment for practitioners.
Assist in the production of learning bulletins/newsletters, ensuring content provides clinical updates for staff; production is timely, and content is quality controlled.
Person Specification
Qualifications
Essential
- Degree in Healthcare related subject.
- Current professional registration
Desirable
- Post basic qualification in leadership and/or management.
Experience
Essential
- Evidence of expert professional/clinical knowledge in an area supplemented by specialist clinical training and CPD.
- Experience of working clinically post registration.
- Evidence of involvement in the development of a program of care, protocols, and audit.
- Evidence of initiative-taking involvement in the development of clinical practice.
Skills
Essential
- Effective communicator able to communicate complex and sensitive information.
- Evidence of effective people management and leadership skills.
- Can demonstrate assertiveness, tact and diplomacy appropriately.
- Computer literacy.
- Must be able to receive and present complex, sensitive or contentious information to large and influential groups.
- Negotiate with stakeholders on difficult and controversial issues including performance and change.
- Demonstrated capability to plan over short, medium, and long-term periods and adjust plans and resource requirements accordingly.
- Experience of project principles techniques or quality improvement programmes.
- Critical thinking skills and ability to respond to sudden unexpected demands.
- Ability to analyse complex facts and situations and develop a range of options.
Knowledge
Essential
- Has the ability to manage conflicting views and reconciles inter and intra professional differences of opinion.
- Working knowledge of the Datix Risk Management system.
- Knowledge of Governance and Risk areas, acquired through post graduate diploma or equivalent experience.
Values
Essential
- Mental effort: To exert frequent concentration - responding to frequent changing operational pressures and to deal with service issues.
- Emotional effort: The post holder will at times be exposed to distressing and occasional highly distressing and emotional circumstances.
Person Specification
Qualifications
Essential
- Degree in Healthcare related subject.
- Current professional registration
Desirable
- Post basic qualification in leadership and/or management.
Experience
Essential
- Evidence of expert professional/clinical knowledge in an area supplemented by specialist clinical training and CPD.
- Experience of working clinically post registration.
- Evidence of involvement in the development of a program of care, protocols, and audit.
- Evidence of initiative-taking involvement in the development of clinical practice.
Skills
Essential
- Effective communicator able to communicate complex and sensitive information.
- Evidence of effective people management and leadership skills.
- Can demonstrate assertiveness, tact and diplomacy appropriately.
- Computer literacy.
- Must be able to receive and present complex, sensitive or contentious information to large and influential groups.
- Negotiate with stakeholders on difficult and controversial issues including performance and change.
- Demonstrated capability to plan over short, medium, and long-term periods and adjust plans and resource requirements accordingly.
- Experience of project principles techniques or quality improvement programmes.
- Critical thinking skills and ability to respond to sudden unexpected demands.
- Ability to analyse complex facts and situations and develop a range of options.
Knowledge
Essential
- Has the ability to manage conflicting views and reconciles inter and intra professional differences of opinion.
- Working knowledge of the Datix Risk Management system.
- Knowledge of Governance and Risk areas, acquired through post graduate diploma or equivalent experience.
Values
Essential
- Mental effort: To exert frequent concentration - responding to frequent changing operational pressures and to deal with service issues.
- Emotional effort: The post holder will at times be exposed to distressing and occasional highly distressing and emotional circumstances.
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Senior Nursing & Governance - E01005
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Senior Nursing & Governance - E01005
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
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Posted 1 month(s) ago
Reference: 413-110117-RI-LM
Job summary
Please note that these posts are permanent contracts at 37.5 hours per week.
We are looking to appoint a Research Practitioner (Band 4) in the Melanoma Research team within The Christie NHS Foundation Trust. The research teams form part of the Research and Innovation division and are made up of a multi-disciplinary group of staff who are dedicated to cancer research and treatment.
We are seeking an enthusiastic, motivated, and experienced individual who will be responsible for assisting the research nurses, consultants and trial management team with the delivery of clinical research projects and clinical trials. We are looking for an individual who is able to demonstrate work experience in data management involving clinical trials, good understanding of clinical research, GCP and clinical trial governance. Strong candidates will have excellent organisation and communication skills, work well both in a team and using their own initiative.
Applicants should meet all the essential criteria on the job description as a minimum. We are looking for a candidate with good organisational and communication skills, with the ability to multi-task. Due to the vital nature of our work and the impact on patients and the research community, attention to detail is an essential skill.
An informal conversation to discuss the post is highly recommended.
Main duties of the job
The post holder will work across both the clinical and administrative functions of the Melanoma Research Team, supporting the delivery of a diverse portfolio of research studies. Clinical duties, undertaken under the supervision of clinical research nurses, will include providing patient support within agreed competencies, collecting biological samples, recording observations, gathering study data, and administering quality of life questionnaires. Administrative responsibilities, supported by the Research Manager, will include managing aspects of clinical research projects, entering patient visit data, responding to study queries, maintaining trial records, filing essential documents, supporting invoicing processes, liaising with pharmaceutical companies, collaborating with the wider R&I team, and assisting with general administrative activities.
Post holders will actively participate in their personal development and appraisal process to achieve role objectives and should hold, or be working towards, the National Care Certificate.
The Melanoma Research Team has a strong collaborative ethos, requiring close working relationships with a wide range of staff. Full training and ongoing development opportunities are provided to support career progression within the Trust. This is a challenging but rewarding role within a supportive, dedicated team committed to excellence in research and patient care.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
03 September 2026
Pay scheme
Agenda for change
Band
Band 4
Salary
£28,392 to £31,157 a year Pro Rata, Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-110117-RI-LM
Job locations
Melanoma - Q01060
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
Provide clinical care for research participants, as delegated by PIs and research nurses, within the boundaries of own knowledge, competence and skill level.Ensure that all research is undertaken according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and Trust policies.Planning and organising day- to-day research and other activitiesConduct delegated data collection with participants, such as questionnaires and interviews.Collection of biological samples as required for the clinical protocol, this may include blood, urine, sputum etc.Preparation of sampling kits as described in study laboratory manuals, maintaining laboratory stock and shipping & tracking of research samples.Undertake research-related activities as required such as clinical observations and NEWS2, blood glucose monitoring, blood sampling (venepuncture and other venous access), PK sampling, cannulation and ECGs.Attend individual project meetings as required.Contribute to clinical and research governance processes, including adverse event and incident reporting, supporting any investigations.Understand and deliver care in accordance with regulatory approved clinical research protocols.Ensure all clinical activities are recorded in appropriate systems in a timely manner.Evening and weekend shifts may occasionally be required to meet the clinical needs of the service.
RESEARCHAct as a point of contact for the core Research and Innovation team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to trial set up and general trial conduct.Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times.Process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines.Complete case report forms as per sponsor requirements, and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits.Cross check, confirm data and complete query resolution with sponsors and third parties in a timely manner.Completion of clinical trial specific databases with data from various sources such as questionnaires, hospital records and other electronic and paper sources.Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature.Ensure that data is available and up to date for any meetings related to a clinical trial.If required attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team.Undertake general administrative tasks related to clinical trials as delegated by your line manager.Assist with preparation for audit and inspections within assigned teams.
KEY VALUESDemonstrates the agreed set of values and accountable for own attitude and behaviour.
Job description
Job responsibilities
Provide clinical care for research participants, as delegated by PIs and research nurses, within the boundaries of own knowledge, competence and skill level.Ensure that all research is undertaken according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and Trust policies.Planning and organising day- to-day research and other activitiesConduct delegated data collection with participants, such as questionnaires and interviews.Collection of biological samples as required for the clinical protocol, this may include blood, urine, sputum etc.Preparation of sampling kits as described in study laboratory manuals, maintaining laboratory stock and shipping & tracking of research samples.Undertake research-related activities as required such as clinical observations and NEWS2, blood glucose monitoring, blood sampling (venepuncture and other venous access), PK sampling, cannulation and ECGs.Attend individual project meetings as required.Contribute to clinical and research governance processes, including adverse event and incident reporting, supporting any investigations.Understand and deliver care in accordance with regulatory approved clinical research protocols.Ensure all clinical activities are recorded in appropriate systems in a timely manner.Evening and weekend shifts may occasionally be required to meet the clinical needs of the service.
RESEARCHAct as a point of contact for the core Research and Innovation team, study sponsors, clinical research organisations and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to trial set up and general trial conduct.Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times.Process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines.Complete case report forms as per sponsor requirements, and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits.Cross check, confirm data and complete query resolution with sponsors and third parties in a timely manner.Completion of clinical trial specific databases with data from various sources such as questionnaires, hospital records and other electronic and paper sources.Liaise with internal and external NHS staff regarding case notes, data collection, archival tumour blocks, mortality data, and other general trial activities, which may be confidential and sensitive in nature.Ensure that data is available and up to date for any meetings related to a clinical trial.If required attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team.Undertake general administrative tasks related to clinical trials as delegated by your line manager.Assist with preparation for audit and inspections within assigned teams.
KEY VALUESDemonstrates the agreed set of values and accountable for own attitude and behaviour.
Person Specification
Qualifications
Essential
- Diploma or relevant experience
Desirable
- A research qualification / clinical research training
- Degree in science or health-related discipline
- National Care certificate (Christie Care Certificate)
Experience
Essential
- Experience of working in a research environment Or Experience working in a healthcare environment
Desirable
- Data management experience
- Clinical research experience
- phlebotomy skills
Skills
Essential
- IT skills. Experience of using Email, Excel, Word and Outlook
Desirable
- Evidence of IT training
- Intra-venous access training, or a willingness to undertake this
Knowledge
Essential
- Awareness of ICH "Good Clinical Practice"
- Knowledge and understanding of patient observations
Desirable
- Knowledge of the clinical trial process
- Understanding of medical terminology and cancer
- Knowledge of patient information systems
Vaues
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Ability to work on own initiative
- Ability to organise and prioritise own workload
- Ability to work as part of a multi-disciplinary team
- Able to work flexibly and to tight deadlines
- Ability to communicate effectively at all levels
Person Specification
Qualifications
Essential
- Diploma or relevant experience
Desirable
- A research qualification / clinical research training
- Degree in science or health-related discipline
- National Care certificate (Christie Care Certificate)
Experience
Essential
- Experience of working in a research environment Or Experience working in a healthcare environment
Desirable
- Data management experience
- Clinical research experience
- phlebotomy skills
Skills
Essential
- IT skills. Experience of using Email, Excel, Word and Outlook
Desirable
- Evidence of IT training
- Intra-venous access training, or a willingness to undertake this
Knowledge
Essential
- Awareness of ICH "Good Clinical Practice"
- Knowledge and understanding of patient observations
Desirable
- Knowledge of the clinical trial process
- Understanding of medical terminology and cancer
- Knowledge of patient information systems
Vaues
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Ability to work on own initiative
- Ability to organise and prioritise own workload
- Ability to work as part of a multi-disciplinary team
- Able to work flexibly and to tight deadlines
- Ability to communicate effectively at all levels
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Employer details
Employer name
The Christie NHS FT
Address
Melanoma - Q01060
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Melanoma - Q01060
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-108542-CNS-LM
Job summary
We are looking for hardworking team players to join us in the friendly Radiotherapy treatment delivery teams at all The Christie sites-Withington, Macclesfield, Oldham and Salford. The Band 6 position is a key member of the treatment team and is encouraged to contribute towards the development of the treatment delivery service. All sites have Elekta LinAcs.
We are looking for experienced radiographers in treatment delivery, who are enthusiastic and motivated to take responsibility for running our treatment machines and managing a diverse workload of patients in the Radiotherapy service. They will be expected to lead and supervise staff operating the equipment under the direct supervision of the Superintendent Radiographers. Successful applicants will have wide experience with radiotherapy equipment and treatment techniques, be highly motivated and have excellent communication andinterpersonal skills. We are looking for applicants with a commitment to developing themselves, the team, and the Radiotherapy Service. HCPC registration required. We look forward to hearing from you. We have several positions available including fixed term and permanent positions. Applications for part-time /full-time and other working patterns welcome We welcome informal enquiries from interested candidates who would like to know more about the role. Shift patterns between 06:00am and 23:00pm
Main duties of the job
To lead, co-ordinate, supervise and manage a team of staff operating radiotherapy equipment and act as lead practitioner, making assessments and key decisions regarding workload management, patient care, and treatment.To ensure that the highly complex radiotherapy and imaging equipment is safe and accurate to operate, both for staff and patients, undertaking the appropriate machine checks, reporting any variances, faults, and malfunctions as necessary.Evaluate delivery of radiotherapy through application and interpretation of treatment verification proceduresFollow appropriate systems and working methods to achieve the safe, timely achievement of workload targets.Be able to accurately position patient and operate highly complex radiotherapy and imaging equipment along the radiotherapy pathway. Keep accurate records and comply with necessary policies and procedures.Analyse systematically and evaluate all data and information relevant to patients' diagnosis, ensuring the patient and their relatives are treated with dignity and respect at all times.Communicate confidential sensitive information, and provide emotional support, to patients and their carers/relatives including children and the terminally ill. Provide information to patients and their carers regarding the radiotherapy pathway and expected side effects.To implement the procedures and work instructions described for the department in the accredited Quality Management System and report any variances.
About us
The Christie is one of Europe's leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country. We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years. We run one of the largest early clinical trial units in Europe with over 300 trials every year. Cancer research in Manchester, most of which is undertaken on the Christie site, has been officially ranked the best in the UK.Our Radiotherapy network has sites based at Withington, Oldham, Macclesfield and Salford; treating approximately 9,500 patients per year over 13 treatment machines.
Details
Date posted
03 September 2026
Pay scheme
Agenda for change
Band
Band 6
Salary
£39,959 to £48,117 a year Pro rata Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-108542-CNS-LM
Job locations
Radiotherapy Withington Treatment - E00079
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
To ensure that the highly complex radiotherapy and imaging equipment is safe and accurate to operate, both for staff and patients, undertaking the appropriate machine checks and reporting any variances, faults, and malfunctions.
Undertake and evaluate radiation dose delivery and complex calculations involving a range of radiation types and energies.
Interpret, monitor, and evaluate the treatment prescriptions to ensure that radiotherapy is delivered accurately and reproducibly and in accordance with the quality system.
Evaluate delivery of radiotherapy through application and interpretation of treatment verification procedures.
Ensure the team follows appropriate systems and working methods to achieve the safe, timely achievement of workload targets.
Accurately position patient and operate highly complex radiotherapy and imaging equipment along the radiotherapy pathway.
Ensure the team keeps accurate records and comply with necessary policies and procedures.
Analyse systematically and evaluate all data and information relevant to patients diagnosis, ensuring the patient and their relatives are treated with dignity and respect at all times.
Communicate confidential sensitive information, and provide emotional support, to patients and their carers/relatives including children and the terminally ill. Provide information to patients and their carers with regard to the radiotherapy pathway and expected side effects.
Communicate accurate and timely information with all other disciplines involved along the patients pathway.
With the team on the unit, patients and the wider multidisciplinary team manage areas of conflict and escalate as necessary.
Anticipate and identify common and complex treatment related side effects, offering advice and where necessary refer to other relevant health care professionals.
Provide, receive, and use sensitive information, maintaining patient confidentiality at all times, in line with information governance legislation.
Apply safe and effective moving and handling skills in order to protect patients and staff and abide by Health and safety legislation in the workplace.
Minimise risk of cross infection through contamination by bodily fluids/matter. In accordance with the infection control policy.
Implement the procedures and work instructions described for the department in accredited quality management system and report any variances.
Contribute to development of the quality management system by reviewing and writing work instructions and operating procedures.
Ensure all work and actions comply with local rules and current UK Ionising Radiation Regulations 1999 and IR(ME)R 2017.
Be aware of and participate in the audit and research within the department and the implementation of new processes and techniques.
Undertake training and competency to dispense medication under Patient Group Direction (PGD).
Participate in the extended shift system, bank holidays, weekend working and on-call.
Any other duties negotiated with the post holder, to develop their role in the organisation.
Achieve all the competencies as outlined by the radiotherapy education team, within a time period as outlined by line manager.
Supervisory & managerial
Lead, co-ordinate, supervise and manage a team of staff operating radiotherapy equipment and act as lead practitioner, making assessments and key decisions in regard to workload management, patient care, and treatment.
Teaching and training
Provide mentorship and guidance for junior staff and be a good role model.
Participate in an annual Personal Development Review.
Attend all essential training and clinical updates as required and ensure your team also attend all relevant training.
Assimilate new ideas and techniques and have an ability to assess their value.
Assist in the supervision and training/teaching of pre-registration students and new members of staff.
Highlight to line manager all issues of inadequate performance, including capability and poor professional standards, for students and employees. Provide evidence where necessary and requested.
Job description
Job responsibilities
To ensure that the highly complex radiotherapy and imaging equipment is safe and accurate to operate, both for staff and patients, undertaking the appropriate machine checks and reporting any variances, faults, and malfunctions.
Undertake and evaluate radiation dose delivery and complex calculations involving a range of radiation types and energies.
Interpret, monitor, and evaluate the treatment prescriptions to ensure that radiotherapy is delivered accurately and reproducibly and in accordance with the quality system.
Evaluate delivery of radiotherapy through application and interpretation of treatment verification procedures.
Ensure the team follows appropriate systems and working methods to achieve the safe, timely achievement of workload targets.
Accurately position patient and operate highly complex radiotherapy and imaging equipment along the radiotherapy pathway.
Ensure the team keeps accurate records and comply with necessary policies and procedures.
Analyse systematically and evaluate all data and information relevant to patients diagnosis, ensuring the patient and their relatives are treated with dignity and respect at all times.
Communicate confidential sensitive information, and provide emotional support, to patients and their carers/relatives including children and the terminally ill. Provide information to patients and their carers with regard to the radiotherapy pathway and expected side effects.
Communicate accurate and timely information with all other disciplines involved along the patients pathway.
With the team on the unit, patients and the wider multidisciplinary team manage areas of conflict and escalate as necessary.
Anticipate and identify common and complex treatment related side effects, offering advice and where necessary refer to other relevant health care professionals.
Provide, receive, and use sensitive information, maintaining patient confidentiality at all times, in line with information governance legislation.
Apply safe and effective moving and handling skills in order to protect patients and staff and abide by Health and safety legislation in the workplace.
Minimise risk of cross infection through contamination by bodily fluids/matter. In accordance with the infection control policy.
Implement the procedures and work instructions described for the department in accredited quality management system and report any variances.
Contribute to development of the quality management system by reviewing and writing work instructions and operating procedures.
Ensure all work and actions comply with local rules and current UK Ionising Radiation Regulations 1999 and IR(ME)R 2017.
Be aware of and participate in the audit and research within the department and the implementation of new processes and techniques.
Undertake training and competency to dispense medication under Patient Group Direction (PGD).
Participate in the extended shift system, bank holidays, weekend working and on-call.
Any other duties negotiated with the post holder, to develop their role in the organisation.
Achieve all the competencies as outlined by the radiotherapy education team, within a time period as outlined by line manager.
Supervisory & managerial
Lead, co-ordinate, supervise and manage a team of staff operating radiotherapy equipment and act as lead practitioner, making assessments and key decisions in regard to workload management, patient care, and treatment.
Teaching and training
Provide mentorship and guidance for junior staff and be a good role model.
Participate in an annual Personal Development Review.
Attend all essential training and clinical updates as required and ensure your team also attend all relevant training.
Assimilate new ideas and techniques and have an ability to assess their value.
Assist in the supervision and training/teaching of pre-registration students and new members of staff.
Highlight to line manager all issues of inadequate performance, including capability and poor professional standards, for students and employees. Provide evidence where necessary and requested.
Person Specification
Qualifications
Essential
- DCR(T), BSc (Hons) or PGDip in Therapeutic Radiography).
- HCPC registration
Desirable
- Attendance at post-registration training events, M-level modules or management/leadership training.
Experience
Essential
- Clinical Experience within a treatment setting demonstrated by evidence of a contemporary range of treatment equipment and techniques including ablative techniques (SRS/SABR).
- Supporting colleagues in managing patients including protocol variations, response to imaging/changes in treatments.
- Experience in on-treatment imaging and relevant on-set clinical decision making.
- Experience of quality, governance and service improvement. Contributing to a ISO9001-accredited system or similar.
- Reporting of incidents, errors, complaints and compliments.
- Participating in technical developments.
- Experience of working within a team environment.
Desirable
- Awareness of contemporary trends in advanced radiotherapy.
- Awareness of clinical practice at other Radiotherapy centres.
- Awareness of trial protocols and procedures .
Skills
Essential
- Ability to manage difficult conversations.
- Ability in conflict resolution with all grades of staff, patients, carers and general public.
- Ability to foster a team-environment, motivating colleagues.
- Ability to impart messages including in group setting, utilising presentation aids as appropriate.
- Ability to manage colleagues.
- Ability to manage workload.
- Ability to manage pathways.
- Ability to analyse data and formulate plans based on these.
- Ability to make sound judgements to support clinical decisions.
- Ability to utilise core clinical IT (e.g. R&V systems, PACS/RIS systems, PAS systems).
- Ability to utilise clinical support IT (e.g. quality management systems, incident reporting systems, audit software).
- Ability to utilise core non-clinical IT (e.g. MS Office etc).
Knowledge
Essential
- Knowledge of the principles of radiotherapy applied to all aspects of the radiotherapy pathway.
- Evidence of radiotherapy physics, anatomy and radiobiological knowledge.
- Understanding of referral pathways and the patient's journey up to, through and beyond radiotherapy.
- Good knowledge of other relevant legislation, guidance and national working parties in radiotherapy.
- Advanced knowledge of IR(ME)R 2017 and IRR 2017 and responsibilities relating to own professional practice.
- Knowledge of Data Protection legislation, health and safety legislation, etc.
- Awareness of the professional context including the role and function of the College of Radiographers, the National Radiotherapy Board and the National Radiotherapy Implementation Group A/I SKILLS.
Values
Essential
- Ability to demonstrate the organisational values and behaviours.
Person Specification
Qualifications
Essential
- DCR(T), BSc (Hons) or PGDip in Therapeutic Radiography).
- HCPC registration
Desirable
- Attendance at post-registration training events, M-level modules or management/leadership training.
Experience
Essential
- Clinical Experience within a treatment setting demonstrated by evidence of a contemporary range of treatment equipment and techniques including ablative techniques (SRS/SABR).
- Supporting colleagues in managing patients including protocol variations, response to imaging/changes in treatments.
- Experience in on-treatment imaging and relevant on-set clinical decision making.
- Experience of quality, governance and service improvement. Contributing to a ISO9001-accredited system or similar.
- Reporting of incidents, errors, complaints and compliments.
- Participating in technical developments.
- Experience of working within a team environment.
Desirable
- Awareness of contemporary trends in advanced radiotherapy.
- Awareness of clinical practice at other Radiotherapy centres.
- Awareness of trial protocols and procedures .
Skills
Essential
- Ability to manage difficult conversations.
- Ability in conflict resolution with all grades of staff, patients, carers and general public.
- Ability to foster a team-environment, motivating colleagues.
- Ability to impart messages including in group setting, utilising presentation aids as appropriate.
- Ability to manage colleagues.
- Ability to manage workload.
- Ability to manage pathways.
- Ability to analyse data and formulate plans based on these.
- Ability to make sound judgements to support clinical decisions.
- Ability to utilise core clinical IT (e.g. R&V systems, PACS/RIS systems, PAS systems).
- Ability to utilise clinical support IT (e.g. quality management systems, incident reporting systems, audit software).
- Ability to utilise core non-clinical IT (e.g. MS Office etc).
Knowledge
Essential
- Knowledge of the principles of radiotherapy applied to all aspects of the radiotherapy pathway.
- Evidence of radiotherapy physics, anatomy and radiobiological knowledge.
- Understanding of referral pathways and the patient's journey up to, through and beyond radiotherapy.
- Good knowledge of other relevant legislation, guidance and national working parties in radiotherapy.
- Advanced knowledge of IR(ME)R 2017 and IRR 2017 and responsibilities relating to own professional practice.
- Knowledge of Data Protection legislation, health and safety legislation, etc.
- Awareness of the professional context including the role and function of the College of Radiographers, the National Radiotherapy Board and the National Radiotherapy Implementation Group A/I SKILLS.
Values
Essential
- Ability to demonstrate the organisational values and behaviours.
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Radiotherapy Withington Treatment - E00079
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Radiotherapy Withington Treatment - E00079
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-110467-CNS-DA
Job summary
An exciting opportunity has arisen for a well-motivated individual to join us as a PA/Medical Secretary in the Oncology Department within Networked Services Division.
This is a part time permanent post. It will be working 22.5 hours per week Monday to Friday, with the option of hybrid working. The Trust are committed to supporting flexible working agreements.
You will be responsible for covering the provisions of full secretarial and administrative support within the CNS (Central Nervous System) team, ensuring a high standard of PA / secretarial duties is maintained and deadlines and audio typing targets are met.
You will be enthusiastic, flexible, willing to learn, eager to play an effective part in a busy team environment, work to a high standard and be able to use your own initiative.
You will have experience of audio typing and copy typing and ideally have worked within a healthcare environment with Medical Secretarial experience and a good knowledge of medical terminology. Knowledge of cancer pathways/targets would be beneficial.
When applying for this position, please refer to the person specification and demonstrate within your application form how you meet the criteria, providing examples where possible.
Main duties of the job
As a PA/Medical Secretary for the CNS (Central Nervous System)Team, you will be responsible for completing, but not limited to, tasks such as:
Liaise with all consultants in your area of responsibility to provide a full secretarial service, including all administrative duties & dealing with mail, this includes placing it in order of priority & acting on matters which can be dealt with without further reference.
Appropriately disseminate a variety of correspondence/documentation, some of which is highly confidential.
Type clinical correspondence, treatment summaries and annotations, ensuring compliance with turnaround time/ targets and ensure that office instructions are followed.Organise and schedule meetings and maintain an up to date diary for appointments, meetings and interviews.
Effectively monitor clinic templates liaising with clinical team and administration staff to ensure clinic numbers are manageable. Escalating to the management team when appropriate.
Liaise with staff at all levels both internally and externally, answering written and verbal enquiries when necessary, taking action on all matters which can be dealt with without further reference.
Answer written and verbal enquiries from patients/relatives, referring enquiries to consultants only when necessary.
Deal with stressful phone calls which can be emotional / abusive & of a sensitive nature from relatives/patients.
Liaise with internal & external departments to arrange clinical investigations/procedures.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
28 August 2026
Pay scheme
Agenda for change
Band
Band 4
Salary
£28,392 to £31,157 a year Pro Rata, Per Annum
Contract
Permanent
Working pattern
Part-time
Reference number
413-110467-CNS-DA
Job locations
Clinical Oncology Admin Support - E00093
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
SPECIFIC DUTIES AND RESPONSIBILITIES: Liaise with all consultants in your area of responsibility to provide a full secretarial service, including all administrative duties and dealing with mail, which includes placing it in order of priority and acting on matters which can be dealt with without further reference. Appropriately disseminate a variety of correspondence/documentation, some of which is highly confidential. Organize and schedule meetings and maintain an up-to-date diary for appointments, meetings and interviews. Effectively monitor clinic templates liaising with clinical team and appropriate administration staff to ensure clinic numbers are manageable. Escalating to Admin and Service Managers when appropriate. Liaise with staff at all levels both internally and externally, answering written and verbal enquiries when necessary, acting on all matters which can be dealt with without further reference. Answer written and verbal enquiries from patients/relatives, referring enquiries to consultants only when necessary. Deal with stressful phone calls which can be emotional / abusive and of a sensitive nature from relatives/patients. Liaise with internal and external departments to arrange clinical investigations/procedures. Liaise with patients involved in trials undertaken by the team, coordinating all necessary information between patients, hospital and organizing bodies. Ensure accurate input of patient details when entering data onto information databases and Patient Administration System (Careflow) including routine use of the case note tracking system. Receive new patient referrals and organize appointment/admissions and arrange treatment as required. Contribute to the appropriate management of the waiting list, particularly in relation to patients who fall within the two-week wait category Co-ordinate annual leave within the group to ensure clinics are capped or cancelled as necessary in order that clinics are managed effectively, and nursing staff are allocated appropriately to other areas. Contribute to the training of new members of staff within a given area as required. Ensure case notes are kept up to date and that all investigations and other material (outside notes and films) are available for clinic appointments/admissions. Provide information required to support the investigation of litigation cases. Provide statistical information to the Information Department as required. Work with Clinicians, Managers and Administration staff to review working practices, identify new improved ways of working and find solutions to problems. Work with the management team to improve quality and range of services, with resources being managed according to agreed policies and priorities. Ensure all relevant information is available for multi-disciplinary meetings for your team. Co-ordinate case notes and reports where necessary. ADDITIONAL REQUIREMENTS
- Always follow risk management procedures including the identification, assessment, and management of risk within the division.
- To abide by all Trust policies and Procedures.
- To be responsible for own professional /personal development, including participating in ongoing appraisal and personal development planning.
Job description
Job responsibilities
SPECIFIC DUTIES AND RESPONSIBILITIES: Liaise with all consultants in your area of responsibility to provide a full secretarial service, including all administrative duties and dealing with mail, which includes placing it in order of priority and acting on matters which can be dealt with without further reference. Appropriately disseminate a variety of correspondence/documentation, some of which is highly confidential. Organize and schedule meetings and maintain an up-to-date diary for appointments, meetings and interviews. Effectively monitor clinic templates liaising with clinical team and appropriate administration staff to ensure clinic numbers are manageable. Escalating to Admin and Service Managers when appropriate. Liaise with staff at all levels both internally and externally, answering written and verbal enquiries when necessary, acting on all matters which can be dealt with without further reference. Answer written and verbal enquiries from patients/relatives, referring enquiries to consultants only when necessary. Deal with stressful phone calls which can be emotional / abusive and of a sensitive nature from relatives/patients. Liaise with internal and external departments to arrange clinical investigations/procedures. Liaise with patients involved in trials undertaken by the team, coordinating all necessary information between patients, hospital and organizing bodies. Ensure accurate input of patient details when entering data onto information databases and Patient Administration System (Careflow) including routine use of the case note tracking system. Receive new patient referrals and organize appointment/admissions and arrange treatment as required. Contribute to the appropriate management of the waiting list, particularly in relation to patients who fall within the two-week wait category Co-ordinate annual leave within the group to ensure clinics are capped or cancelled as necessary in order that clinics are managed effectively, and nursing staff are allocated appropriately to other areas. Contribute to the training of new members of staff within a given area as required. Ensure case notes are kept up to date and that all investigations and other material (outside notes and films) are available for clinic appointments/admissions. Provide information required to support the investigation of litigation cases. Provide statistical information to the Information Department as required. Work with Clinicians, Managers and Administration staff to review working practices, identify new improved ways of working and find solutions to problems. Work with the management team to improve quality and range of services, with resources being managed according to agreed policies and priorities. Ensure all relevant information is available for multi-disciplinary meetings for your team. Co-ordinate case notes and reports where necessary. ADDITIONAL REQUIREMENTS
- Always follow risk management procedures including the identification, assessment, and management of risk within the division.
- To abide by all Trust policies and Procedures.
- To be responsible for own professional /personal development, including participating in ongoing appraisal and personal development planning.
Person Specification
Qualifications
Essential
- 5 GCSE's grade C or above including Maths and English or equivalent
Desirable
- RSA stage II or III
- AMSPAR Diploma (or equivalent)
Experience
Essential
- Previous secretarial/admin experience
- Experience of working in a health care setting
- Experience of working as part of a team and in isolation
- Experience in managing priorities under pressure, to meet service needs and strict deadlines
Desirable
- Previous secretarial experience in Oncology
- Previous experience of patient management systems
Skills
Essential
- Audio and copy typing
- Sound knowledge of medical terminology
- Word-processing
- Willing to attend training courses appropriate to role
Desirable
- Microsoft Office (Excel, PowerPoint)
Knowledge
Essential
- Excellent communication skills
- Ability to produce accurate, well presented work
- Ability to work as part of a team
- Organisational abilities to work to tight deadlines
- Ability to work on own and to use initiative
- Ability to work under pressure
- Reliability
- Flexibility to work within the team where necessary
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Excellent interpersonal skills
- Flexible and pro-active approach
- Self-motivated and Enthusiastic
Person Specification
Qualifications
Essential
- 5 GCSE's grade C or above including Maths and English or equivalent
Desirable
- RSA stage II or III
- AMSPAR Diploma (or equivalent)
Experience
Essential
- Previous secretarial/admin experience
- Experience of working in a health care setting
- Experience of working as part of a team and in isolation
- Experience in managing priorities under pressure, to meet service needs and strict deadlines
Desirable
- Previous secretarial experience in Oncology
- Previous experience of patient management systems
Skills
Essential
- Audio and copy typing
- Sound knowledge of medical terminology
- Word-processing
- Willing to attend training courses appropriate to role
Desirable
- Microsoft Office (Excel, PowerPoint)
Knowledge
Essential
- Excellent communication skills
- Ability to produce accurate, well presented work
- Ability to work as part of a team
- Organisational abilities to work to tight deadlines
- Ability to work on own and to use initiative
- Ability to work under pressure
- Reliability
- Flexibility to work within the team where necessary
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Excellent interpersonal skills
- Flexible and pro-active approach
- Self-motivated and Enthusiastic
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Clinical Oncology Admin Support - E00093
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Clinical Oncology Admin Support - E00093
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
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Posted 1 month(s) ago
Reference: 413-110495-RI-DA
Job summary
We are looking for a highly motivated nurse to join the Experimental Cancer Medicine Team (ECMT) at The Christie NHS Foundation Trust. ECMT supports a growing portfolio of early phase research studies both commercial and investigator led, including first in human drug trials.The post holder will work alongside a team of physicians, research nurses & clinical trial administrators on a portfolio of trials providing support to patients, administering trial treatments & carrying out trial assessments for patients on study.
Research nursing is an exciting and developing role, supported through the R&I division with a good education and development package in place to ensure that staff reach their potential.
Central to this role is the responsibility of assessing and managing the care pathways including the delivery of all specified treatments for participants in research within a multidisciplinary team. Key responsibilities of the post include the coordination of the trial protocols and support for cancer patients.
A background in oncology, flexibility in working, excellent communication and interpersonal skills are essential. Experience in clinical research would be desirable but not essential.An informal discussion about the post is strongly recommended with the possibility to spend some time with the team to understand better the requirement of the role.
Please note this advert may close earlier if adequate number of applicants.
Main duties of the job
The CRN will be involved in every stage of the portfolio activities including feasibility reviews of new clinical trial opportunities, set-up and activation of new trials, patient recruitment and management, supporting team with data query resolution, reviewing protocol amendments, providing patient-centred insights to the research delivery team by supporting both the patients and the team through all aspects of clinical research of the portfolio.
With support from the team the CRN will ensure that the safety and wellbeing of the patients is maintained within the requirement of the multi-regulatory frameworks for clinical research ensuring compliance with ICH/GCP standards and Trust SOPs.
Line management responsibility for junior staff including supporting them in ensuring research data is collected with compliance to GCP and other regulatory legislation.
Raise the profile of the clinical research nurse and clinical trials within the trust by engaging in promotional events relating to clinical research with attendance and contributions at local, national, and international meetings.
Demonstrate awareness and contribution to divisional, Trust and national objectives and strategies.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
28 August 2026
Pay scheme
Agenda for change
Band
Band 6
Salary
£39,959 to £48,117 a year Pro Rata, Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-110495-RI-DA
Job locations
Phase 1 - Q01312
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
Clinical Research Co-ordination
Work autonomously in all areas of practice relating to clinical research. Understand and deliver care in accordance with regulatory approved clinical research protocols. Understand the process for obtaining NHS permissions (R&D approval) for conducting clinical trials at site. As project lead, ensure permissions are in place prior to any patient recruitment. Participate in clinical trial feasibilities and risk assessments of clinical trial protocols. Ensure all clinical trial activities are recorded in appropriate systems in a timely manner. Awareness of trial specific, regional and national targets. Identify and implement strategies for recruiting patients to clinical trials ensuring that targets for patient recruitment are delivered. Delegation and oversight of research related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP. Arrange and facilitate clinical trial related meetings. Involvement in appropriate financial remunerations for clinical trial activity.
Clinical Service and Professional ResponsibilitiesAssimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives, and carers regarding prognosis Contribute to the development, implementation, and review of specialist care pathways in conjunction with appropriate personnel. Demonstration of expert knowledge in specialist area to maintain clinical excellence. Demonstrate awareness of divisional and trust strategic objectives including performance indicators and metrics. Escalation of governance issues impacting on delivery of job purpose. To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals. Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training in accordance with local policy. Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Code of Practice Conduct and current best practice. Development and maintenance of a high-quality service by: Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial. Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention. Contribute to development of specialist Standard Operating Procedures and guidelines. Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients. Participate in monitoring and audit activities within research team To carry out non-medical prescribing within scope of professional practice and in accordance with local policies and procedures and national legislation (optional and depending on clinical service needs).
Personal Education, Training and Development Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning. Promote the role of the clinical research nurse as an integral part of the healthcare system. Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development. Participation in trust-wide education programmes and study days. Obtain clinical supervision as appropriate. To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes. Attendance at team and divisional meeting
Staff Management and DevelopmentTo Support the Senior Clinical Research Nurse in the induction and continued supervision of junior members of staff, ensuring compliance with regulatory compliance and legislation. Support the development of specialist study days within own research team. Assist in the provision of specialist education and training in relation to clinical trials to all key stakeholders. Disseminate information by attendance and /or presentations at local, national and international conferences/meetings Contribute to the development of members of the research team
EU DIRECTIVE ICH/GCPAll personnel involved in clinical research have a responsibility to ensure that clinical trials are conducted in accordance with the EU Directive and ICH/GCP.
Job description
Job responsibilities
Clinical Research Co-ordination
Work autonomously in all areas of practice relating to clinical research. Understand and deliver care in accordance with regulatory approved clinical research protocols. Understand the process for obtaining NHS permissions (R&D approval) for conducting clinical trials at site. As project lead, ensure permissions are in place prior to any patient recruitment. Participate in clinical trial feasibilities and risk assessments of clinical trial protocols. Ensure all clinical trial activities are recorded in appropriate systems in a timely manner. Awareness of trial specific, regional and national targets. Identify and implement strategies for recruiting patients to clinical trials ensuring that targets for patient recruitment are delivered. Delegation and oversight of research related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP. Arrange and facilitate clinical trial related meetings. Involvement in appropriate financial remunerations for clinical trial activity.
Clinical Service and Professional ResponsibilitiesAssimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives, and carers regarding prognosis Contribute to the development, implementation, and review of specialist care pathways in conjunction with appropriate personnel. Demonstration of expert knowledge in specialist area to maintain clinical excellence. Demonstrate awareness of divisional and trust strategic objectives including performance indicators and metrics. Escalation of governance issues impacting on delivery of job purpose. To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals. Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training in accordance with local policy. Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Code of Practice Conduct and current best practice. Development and maintenance of a high-quality service by: Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial. Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention. Contribute to development of specialist Standard Operating Procedures and guidelines. Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients. Participate in monitoring and audit activities within research team To carry out non-medical prescribing within scope of professional practice and in accordance with local policies and procedures and national legislation (optional and depending on clinical service needs).
Personal Education, Training and Development Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning. Promote the role of the clinical research nurse as an integral part of the healthcare system. Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development. Participation in trust-wide education programmes and study days. Obtain clinical supervision as appropriate. To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes. Attendance at team and divisional meeting
Staff Management and DevelopmentTo Support the Senior Clinical Research Nurse in the induction and continued supervision of junior members of staff, ensuring compliance with regulatory compliance and legislation. Support the development of specialist study days within own research team. Assist in the provision of specialist education and training in relation to clinical trials to all key stakeholders. Disseminate information by attendance and /or presentations at local, national and international conferences/meetings Contribute to the development of members of the research team
EU DIRECTIVE ICH/GCPAll personnel involved in clinical research have a responsibility to ensure that clinical trials are conducted in accordance with the EU Directive and ICH/GCP.
Person Specification
Qualifications
Essential
- Registered General Nurse -Currently registered with the Nursing & Midwifery Council.
- First Degree or relevant clinical experience
Desirable
- Post-graduate qualification in oncology and/or clinical research
- GCP/ICH recognised recent training
Experience
Essential
- Experience of oncology nursing
- Experience of working autonomously and as part of a Multi-disciplinary team
- Ability to demonstrate evidence of service improvement
Desirable
- Experience of working in a clinical research environment
Skills
Essential
- Highly effective communication skills
- Advance organisational skills
- Good written and analytical skills
- Able to manage work autonomously and manage own workload
- Demonstrable IT Skills - able to use Word, PowerPoint, Excel and Outlook
Desirable
- Intra-venous access and cannulation skills administration of IV chemotherapy
- Good presentation skills
Knowledge
Essential
- Knowledge of the clinical trial process
- Knowledge of ICH-GCP & research governance framework
- Knowledge of professional and NHS issues and policy relating to specialist area
Desirable
- Knowledge of Research Ethics Committees
- Knowledge of the purpose of clinical research
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Maintain professional development and have an awareness of current nursing issues
- Demonstrates flexibility in working hours
Desirable
- Assertiveness2
Person Specification
Qualifications
Essential
- Registered General Nurse -Currently registered with the Nursing & Midwifery Council.
- First Degree or relevant clinical experience
Desirable
- Post-graduate qualification in oncology and/or clinical research
- GCP/ICH recognised recent training
Experience
Essential
- Experience of oncology nursing
- Experience of working autonomously and as part of a Multi-disciplinary team
- Ability to demonstrate evidence of service improvement
Desirable
- Experience of working in a clinical research environment
Skills
Essential
- Highly effective communication skills
- Advance organisational skills
- Good written and analytical skills
- Able to manage work autonomously and manage own workload
- Demonstrable IT Skills - able to use Word, PowerPoint, Excel and Outlook
Desirable
- Intra-venous access and cannulation skills administration of IV chemotherapy
- Good presentation skills
Knowledge
Essential
- Knowledge of the clinical trial process
- Knowledge of ICH-GCP & research governance framework
- Knowledge of professional and NHS issues and policy relating to specialist area
Desirable
- Knowledge of Research Ethics Committees
- Knowledge of the purpose of clinical research
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Maintain professional development and have an awareness of current nursing issues
- Demonstrates flexibility in working hours
Desirable
- Assertiveness2
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Phase 1 - Q01312
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Phase 1 - Q01312
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-110341-RI-TM
Job summary
An exciting opportunity has arisen for an experienced research professional to join The Christie Research and Innovation Division as a Research Quality Assurance Manager. This key role supports the delivery of high-quality, safe and regulatory compliant research across the Trust Sponsored Research Portfolio.
Working within the Research Quality and Regulatory Compliance Team, you will have a specific focus on Sponsor oversight, leading the development, maintenance and continuous improvement of the Trust Sponsor Quality Management System (QMS). You will help ensure sponsored research is conducted in accordance with applicable regulations, Good Clinical Practice and organisational standards.You will deliver risk-based quality assurance activities, audits, compliance reviews and quality improvement initiatives, providing assurance that Sponsor processes remain effective and inspection ready. Working with investigators, research teams and key stakeholders, you will promote a culture of quality, continuous improvement and organisational learning.
The successful candidate will have substantial experience in research quality assurance, governance or regulatory compliance, together with a strong understanding of Good Clinical Practice, Sponsor responsibilities and quality management systems.
This is an opportunity to play a pivotal role in strengthening Sponsor oversight, participant safety and research excellence within one of the UK's leading cancer centres.
Main duties of the job
The post holder will lead the operational management of the Research Quality Management System (QMS), ensuring quality processes, documentation, audit activity, corrective and preventative actions (CAPAs), quality metrics and assurance records are maintained to a high standard. Working closely with research teams, investigators and research support services, you will promote a culture of continuous improvement, quality by design, shared learning and accountability.
You will deliver a programme of risk-based quality assurance activities, including audits, quality reviews, compliance assessments and monitoring of improvement actions. Using quality intelligence and performance data, you will identify emerging risks, trends and opportunities for improvement, providing specialist advice to support regulatory compliance and organisational assurance.
The successful candidate will have significant experience in clinical research quality assurance, governance or regulatory compliance, with excellent knowledge of Good Clinical Practice, clinical research regulations and quality management systems. You will possess strong analytical, communication and influencing skills and be able to work collaboratively with a wide range of stakeholders.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
28 August 2026
Pay scheme
Agenda for change
Band
Band 7
Salary
£49,387 to £56,515 a year Pro Rate, Per Annum
Contract
Permanent
Working pattern
Full-time
Reference number
413-110341-RI-TM
Job locations
R&D Office - Q01552
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
1.0 Quality Management and Leadership
Manage the operational delivery of the Trust Sponsored Research Quality Management System. Provide specialist expertise and operational leadership in the implementation, maintenance and continual improvement of research quality management processes. Responsible for making recommendations, providing advice and able to prepare strategic reports/briefings for the Head of Department, steering/reference groups and others as required. Responsible for ensuring the coordination of change control processes within the Trust sponsored research team. Work collaboratively with research support operations and governance teams by maintaining an awareness of quality issues and contributing to problem solving to ensure the delivery of high-quality research. Implement a programme of risk-based quality assurance and assuranceactivities, including audits, quality reviews, compliance assessments andthematic reviews Responsible for leading in the conduct of third-party suppliers/vendor qualification assessments (due diligence) related to Trust sponsored studies. Seeking advice and guidance where necessary. Receive and respond to complex and occasionally sensitive research governance and reported quality related issues Recognise and act upon departures from legislative and research governance requirements, including failure to follow protocols and/or SOPs, responding appropriately and escalating action as required. Support quality reviews and investigations relating to significant quality and compliance concerns, escalating findings appropriately in accordance with Trust procedures. Provide guidance to research operations/governance teams on the interpretation of corporate and regulatory requirements (standard/policies/procedures) related to quality assurance and GCP. Maintain accurate quality management records that are ready for inspection by regulatory authorities on demand. Support the implementation and ongoing evaluation of risk-based quality management approaches across the Trust sponsored research portfolio. Contribute to the identification and review of critical-to-quality factors and quality risks throughout the research lifecycle. Maintain oversight of quality events, deviations, audit findings, CAPAs, lessons learned and compliance trends across the sponsored portfolio. Monitor quality metrics and key performance indicators and provide reports to support organisational assurance. Ensure controlled documents are reviewed and maintained in accordance with document governance requirements. Support the implementation and monitoring of risk-based quality management processes across the sponsored research portfolio.
2.0 Service Improvement /Policy DevelopmentTo develop and implement business processes and Standard OperatingProcedures to ensure that the Trust conforms to the requirements of relevant legislation. Responsible for interpreting, proposing and drafting changes to policies, guidelines and service level agreements (SLAs) which impact the service. Maintain a good knowledge of emerging policies from government departments and external bodies which may impact the service. Promote Quality by Design principles through the development, review and continual improvement of quality systems and research processes Contribute to strategic and contingency planning for the service, which may have an impact on other areas. Foster an environment for continuous improvement through ensuring that lessons learned through audits and inspections are shared within the Department and beyond as necessary. Provide regular reports on quality trends, compliance risk, observations and suggestions to senior management as necessary. Work collaboratively with Research Governance, Sponsorship, Research Delivery and Support Services to identify and implement quality improvement priorities arising from audits, compliance reviews, quality metrics and lessons learned.
3.0 Risk ManagementSupport the departmental lead in ensuring that risk registers are effectively managed and maintained within the Division by ensuring effective processes are implemented for the review of risks within the Trust sponsored research function Maintain oversight of quality and compliance risks identified across the Trust sponsored research portfolio, ensuring appropriate escalation and monitoring through established governance processes.
4.0 CommunicationProvide, receive and analyse highly complex, sensitive and contentiousinformation and make judgements based on the information. Present complex information to a wide range of stakeholders in formal and informal settings. Responsible for providing management reports on Quality Management activities to departmental, Divisional and Trust Governance groups, as required. Present audit findings, compliance trends and quality improvementrecommendations in a constructive and solutions-focused manner. Develop effective working relationships with investigators, research teams and support services to promote engagement with quality improvement activities. Produce routine and ad hoc quality assurance reports for governance groups and senior stakeholders Committed to working and engaging constructively with internal and external stakeholders on a range of business sensitive issues Maintain strong relationships and positive communication channels with other key personnel. Develop and establish research relationships with key partners including academia, NHS and commercial companies. Represent the Research Quality, Assurance and Regulatory Compliance team at relevant quality. Regulatory and governance forums as delegated.
5.0 People Management and DevelopmentProvide professional support, coaching and subject matter expertise to research staff in relation to quality management systems, Good Clinical Practice, audit readiness and compliance requirements. Where required, supervise designated staff, trainees or project-based quality resources. Influence, support, co-ordinate and take the initiative to obtain co-operation or agreement to alter ways of working, particularly where the need for change cannot easily be identified. Provide leadership and standards of best practice, promoting ethical and professional practice throughout the organisation Provide specialist advice to internal and external investigators/ collaborators in the planning of compliant clinical research. Considering the advice of functional leads, determine the quality system training needs of staff in relation to quality systems, deliver area specific training ensuring that there are mechanisms for effective oversight to facilitate departmental and functional leads in ensuring that all staff members are trained appropriately.
6.0 Learning and DevelopmentEnsure own professional knowledge is regularly updated and keep abreast of relevant developments, making effective use of learning opportunities and actively promoting the workplace as a learning environment. Maintaining and developing knowledge of national and local clinical and research quality initiatives Participate in personal objective setting and review, including the creation of a personal development plan. Actively seek mentorship/supervision/coaching to enable reflection and own personal development within the role. Committed to working and engaging constructively with internal and external stakeholders on a range of business sensitive issues
Job description
Job responsibilities
1.0 Quality Management and Leadership
Manage the operational delivery of the Trust Sponsored Research Quality Management System. Provide specialist expertise and operational leadership in the implementation, maintenance and continual improvement of research quality management processes. Responsible for making recommendations, providing advice and able to prepare strategic reports/briefings for the Head of Department, steering/reference groups and others as required. Responsible for ensuring the coordination of change control processes within the Trust sponsored research team. Work collaboratively with research support operations and governance teams by maintaining an awareness of quality issues and contributing to problem solving to ensure the delivery of high-quality research. Implement a programme of risk-based quality assurance and assuranceactivities, including audits, quality reviews, compliance assessments andthematic reviews Responsible for leading in the conduct of third-party suppliers/vendor qualification assessments (due diligence) related to Trust sponsored studies. Seeking advice and guidance where necessary. Receive and respond to complex and occasionally sensitive research governance and reported quality related issues Recognise and act upon departures from legislative and research governance requirements, including failure to follow protocols and/or SOPs, responding appropriately and escalating action as required. Support quality reviews and investigations relating to significant quality and compliance concerns, escalating findings appropriately in accordance with Trust procedures. Provide guidance to research operations/governance teams on the interpretation of corporate and regulatory requirements (standard/policies/procedures) related to quality assurance and GCP. Maintain accurate quality management records that are ready for inspection by regulatory authorities on demand. Support the implementation and ongoing evaluation of risk-based quality management approaches across the Trust sponsored research portfolio. Contribute to the identification and review of critical-to-quality factors and quality risks throughout the research lifecycle. Maintain oversight of quality events, deviations, audit findings, CAPAs, lessons learned and compliance trends across the sponsored portfolio. Monitor quality metrics and key performance indicators and provide reports to support organisational assurance. Ensure controlled documents are reviewed and maintained in accordance with document governance requirements. Support the implementation and monitoring of risk-based quality management processes across the sponsored research portfolio.
2.0 Service Improvement /Policy DevelopmentTo develop and implement business processes and Standard OperatingProcedures to ensure that the Trust conforms to the requirements of relevant legislation. Responsible for interpreting, proposing and drafting changes to policies, guidelines and service level agreements (SLAs) which impact the service. Maintain a good knowledge of emerging policies from government departments and external bodies which may impact the service. Promote Quality by Design principles through the development, review and continual improvement of quality systems and research processes Contribute to strategic and contingency planning for the service, which may have an impact on other areas. Foster an environment for continuous improvement through ensuring that lessons learned through audits and inspections are shared within the Department and beyond as necessary. Provide regular reports on quality trends, compliance risk, observations and suggestions to senior management as necessary. Work collaboratively with Research Governance, Sponsorship, Research Delivery and Support Services to identify and implement quality improvement priorities arising from audits, compliance reviews, quality metrics and lessons learned.
3.0 Risk ManagementSupport the departmental lead in ensuring that risk registers are effectively managed and maintained within the Division by ensuring effective processes are implemented for the review of risks within the Trust sponsored research function Maintain oversight of quality and compliance risks identified across the Trust sponsored research portfolio, ensuring appropriate escalation and monitoring through established governance processes.
4.0 CommunicationProvide, receive and analyse highly complex, sensitive and contentiousinformation and make judgements based on the information. Present complex information to a wide range of stakeholders in formal and informal settings. Responsible for providing management reports on Quality Management activities to departmental, Divisional and Trust Governance groups, as required. Present audit findings, compliance trends and quality improvementrecommendations in a constructive and solutions-focused manner. Develop effective working relationships with investigators, research teams and support services to promote engagement with quality improvement activities. Produce routine and ad hoc quality assurance reports for governance groups and senior stakeholders Committed to working and engaging constructively with internal and external stakeholders on a range of business sensitive issues Maintain strong relationships and positive communication channels with other key personnel. Develop and establish research relationships with key partners including academia, NHS and commercial companies. Represent the Research Quality, Assurance and Regulatory Compliance team at relevant quality. Regulatory and governance forums as delegated.
5.0 People Management and DevelopmentProvide professional support, coaching and subject matter expertise to research staff in relation to quality management systems, Good Clinical Practice, audit readiness and compliance requirements. Where required, supervise designated staff, trainees or project-based quality resources. Influence, support, co-ordinate and take the initiative to obtain co-operation or agreement to alter ways of working, particularly where the need for change cannot easily be identified. Provide leadership and standards of best practice, promoting ethical and professional practice throughout the organisation Provide specialist advice to internal and external investigators/ collaborators in the planning of compliant clinical research. Considering the advice of functional leads, determine the quality system training needs of staff in relation to quality systems, deliver area specific training ensuring that there are mechanisms for effective oversight to facilitate departmental and functional leads in ensuring that all staff members are trained appropriately.
6.0 Learning and DevelopmentEnsure own professional knowledge is regularly updated and keep abreast of relevant developments, making effective use of learning opportunities and actively promoting the workplace as a learning environment. Maintaining and developing knowledge of national and local clinical and research quality initiatives Participate in personal objective setting and review, including the creation of a personal development plan. Actively seek mentorship/supervision/coaching to enable reflection and own personal development within the role. Committed to working and engaging constructively with internal and external stakeholders on a range of business sensitive issues
Person Specification
Qualifications
Essential
- First degree in life sciences discipline or equivalent specialised professional experience
Desirable
- Post graduate qualification in related discipline
- Evidence of Continuing Professional Development
Experience
Essential
- Previous experience in the management of quality assurance and / or regulatory compliance in a research setting within the NHS or Academic setting
- Experience of writing quality System policies and procedures
- Experience in implementation of GCP
Desirable
- Experience of developing strategies, policies, and business plans
Skills
Essential
- Ability to assess and interpret highly complicated and conflicting information and use judgement where appropriate
- Excellent verbal, written and presentation skills
- Possess developed persuasive, motivational, negotiating, empathic or re-assurance skills
- Ability to write and present complex reports and to critically analyse and communicate ideas in complex situations
- Good organisational and time management skills
- Excellent cross disciplinary / interagency communication skills and ability to facilitate collaborative working relationships
- Ability to influence and negotiate others in a challenging environment
- IT, information, project and time management skills
- Ability to deal with difficult / sensitive situations
- Ability to work as part of a team, demonstrated coaching/mentoring skills, good problem resolution skills
- Able to develop and deliver staff training programmes and conference presentations
- Highly developed problem-solving skills and ability to respond to sudden unexpected demands
- Must be able to use initiative to decide relevant actions and make recommendations to Sponsor/Manager, with the aim of improving deliverables and compliance to policies
- Strategic thinking - ability to anticipate and resolve problems before they arise
Knowledge
Essential
- Detailed knowledge of ICH E6(R3) Good Clinical Practice principles
- Knowledge of UK Clinical Trials Regulations and associated guidance
- Knowledge of Quality Management Systems and quality assurance methodologies
- Knowledge of risk-based quality management principles
- Knowledge of CAPA management and root cause analysis methodologies
- Knowledge of audit, assurance and inspection processes
- Understanding of sponsor responsibilities within NHS sponsored research
- Knowledge of research governance frameworks applicable to clinical research
Desirable
- Knowledge of NHS R&D Strategy and NHS research agenda
- Experience of risk management
- Knowledge of Quality by Design principles
- Knowledge of electronic quality management systems
- Knowledge of computerised systems and data integrity principles
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Strong Personal integrity
- Innovative and positive approach
- Flexible and motivated team player
- Occasional travel to other sites
- Elevated level of emotional intelligence
Person Specification
Qualifications
Essential
- First degree in life sciences discipline or equivalent specialised professional experience
Desirable
- Post graduate qualification in related discipline
- Evidence of Continuing Professional Development
Experience
Essential
- Previous experience in the management of quality assurance and / or regulatory compliance in a research setting within the NHS or Academic setting
- Experience of writing quality System policies and procedures
- Experience in implementation of GCP
Desirable
- Experience of developing strategies, policies, and business plans
Skills
Essential
- Ability to assess and interpret highly complicated and conflicting information and use judgement where appropriate
- Excellent verbal, written and presentation skills
- Possess developed persuasive, motivational, negotiating, empathic or re-assurance skills
- Ability to write and present complex reports and to critically analyse and communicate ideas in complex situations
- Good organisational and time management skills
- Excellent cross disciplinary / interagency communication skills and ability to facilitate collaborative working relationships
- Ability to influence and negotiate others in a challenging environment
- IT, information, project and time management skills
- Ability to deal with difficult / sensitive situations
- Ability to work as part of a team, demonstrated coaching/mentoring skills, good problem resolution skills
- Able to develop and deliver staff training programmes and conference presentations
- Highly developed problem-solving skills and ability to respond to sudden unexpected demands
- Must be able to use initiative to decide relevant actions and make recommendations to Sponsor/Manager, with the aim of improving deliverables and compliance to policies
- Strategic thinking - ability to anticipate and resolve problems before they arise
Knowledge
Essential
- Detailed knowledge of ICH E6(R3) Good Clinical Practice principles
- Knowledge of UK Clinical Trials Regulations and associated guidance
- Knowledge of Quality Management Systems and quality assurance methodologies
- Knowledge of risk-based quality management principles
- Knowledge of CAPA management and root cause analysis methodologies
- Knowledge of audit, assurance and inspection processes
- Understanding of sponsor responsibilities within NHS sponsored research
- Knowledge of research governance frameworks applicable to clinical research
Desirable
- Knowledge of NHS R&D Strategy and NHS research agenda
- Experience of risk management
- Knowledge of Quality by Design principles
- Knowledge of electronic quality management systems
- Knowledge of computerised systems and data integrity principles
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Strong Personal integrity
- Innovative and positive approach
- Flexible and motivated team player
- Occasional travel to other sites
- Elevated level of emotional intelligence
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Employer details
Employer name
The Christie NHS FT
Address
R&D Office - Q01552
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
R&D Office - Q01552
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
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Posted 1 month(s) ago
Reference: 413-MD-C2026-25159-DM
Job summary
We are seeking an ambitious, innovative individual with a specific interest in cancer imaging and/or colorectal cancers / MR imaging to work on the "Improving Outcomes in Colorectal Cancer with Peritoneal Metastases: PREDICT-PM (PRE-operative Diagnostic Imaging in Colorectal cancer with Peritoneal Metastases" study.
This research project will address a critical gap in the pre-operative management of appendiceal neoplasms. Whilst the Peritoneal Cancer Index (PCI) is currently the gold standard for assessing disease burden, its radiological application (rPCI) remains inconsistent and technically challenging. The primary objective is to evaluate the diagnostic accuracy, inter-observer reliability, and predictive value of a standardized CT-PCI atlas in patients with non-mucinous appendiceal adenocarcinomas.
The post holder will be supported with dedicated research time (40% of the role) by Dr Joe Mercer and Dr Rohit Kochhar leading the research project and accountable to the Radiology Clinical Tutor for Fellows, and then to the Clinical Director. Clinical duties will include oncological CT, MRI and PET/CT reporting, under consultant supervision as appropriate, Peritoneal MRI reporting and participation in Peritoneal Tumour Service MDT meetings. They will also have the benefit of working alongside a peer group of other Radiology Fellows, as well as close working with the Consultant Radiologist's
Main duties of the job
The appointee will be based at The Christie, Withington Campus. Clinically they will provide senior input to education and training in specialist cancer imaging, including sub-specialisms in CT and MR. The post holder will be supported in producing imaging reports and in further enhancing their involvement with specialist MDTs. Within Research they will lead project to evaluate the diagnostic accuracy, inter-observer reliability, and predictive value of a standardized CT-PCI atlas in patients with non-mucinous appendiceal adenocarcinoma.
The post holder's routine clinical work will initially be closely supervised but they will practice increasingly independently as their experience develops during the year. In turn, the post holder will be able to supervise trainee Radiologists as time and expertise progress.
About us
The Christie is one of Europe's leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country. We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years. We run one of the largest early clinical trial units in Europe with over 300 trials every year. Cancer research in Manchester, most of which is undertaken on the Christie site, has been officially ranked the best in the UK.
The postholder will contribute to the delivery of high quality consultant led care across 7 days. This includes participation in planned weekend and weekday clinical activity to support safe, timely decision making and continuity of care for patients
Details
Date posted
28 August 2026
Pay scheme
Hospital medical and dental staff
Grade
Doctor - other
Salary
£55,355 to £76,582 a year per annum
Contract
Fixed term
Duration
12 months
Working pattern
Full-time
Reference number
413-MD-C2026-25159-DM
Job locations
Radiology - E00298
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIESThe medical establishment consists of 27 Consultants, 3 Clinical Fellows in Oncology Imaging, 1 Clinical Fellow in Interventional Radiology and up to 5 Specialist Trainees in Clinical Radiology. The directorate also collaborates with 3 additional Consultants from other GM Trusts that support PET-CT reporting.
The Clinical Director has professional responsibility for medical staff and clinical responsibility for the Radiology service. They are supported by the Lead Consultants in CT, MR, US, Interventional Radiology, Nuclear Medicine, General Radiology, Clinical Audit and Information Technology and by the clinical tutors for the specialist trainees and fellows.
The appointee will be based at The Christie and will provide senior input to education and training in specialist cancer imaging, including sub-specialisms in CT and MR. The post holder will be supported in producing imaging reports and in further enhancing their involvement with specialist MDTs. Within Research they will lead project to evaluate the diagnostic accuracy, inter-observer reliability, and predictive value of a standardized CT-PCI atlas in patients with non-mucinous appendiceal adenocarcinoma.
The post holders routine clinical work will initially be closely supervised but they will practice increasingly independently as their experience develops during the year. In turn, the post holder will be able to supervise trainee Radiologists as time and expertise progress.
The significant proportion of time dedicated to research will be supported by dedicated research time by Dr Joe Mercer and Dr Rohit Kochhar, and the successful candidate is expected to contribute to projects leading to scientific publications, as well as presentations at national and international meetings.
Teaching Commitment:The department is active in teaching radiology trainees on the North-West training scheme, with further commitments to national and regional radiology teaching. Medical student, FY/CMT and non-radiology ST-teaching is also supported. The post holder will undertake lectures and tutorials to medical and non-medical staff in collaboration with and independent of colleagues.
Multi-Disciplinary Team Meetings:The Consultant Radiologists support the provision of around 25 separate MDT meetings. The post holder will be expected to participate in MDTs, with subspecialist interests accommodated.
Clinical Governance:The post-holder will be expected to participate in all relevant aspects of clinical governance, including maintaining and improving protocols, the consent process, discrepancy reporting, guidelines and clinical audit in conjunction with the other staff in the department. In addition, opportunities exist to be involved with national audit programs of the relevant specialist societies.
Office and Secretarial:The Trust will provide shared office space with other radiology trainees and fellows. Secretarial support is shared between consultants and trainees / fellows.
Continuing Professional DevelopmentThe Trust supports the requirements for continuing professional development (CPD) as laid down by the GMC and surgical colleges and is committed to providing time and financial support for these activities.
Role PlanningBoth part-time and full-time applications will be considered. The post will be offered as 40 hours per week, divided into 20 hours of direct clinical care, 16 hours dedicated research time and 4 hours of supporting activities; this will be reduced proportionally for part-time applications.An indicative timetable is described below (each session lasting 4 hours). Please note that an individualized timetable will be agreed with the Clinical Director, and the fellow supervisor. The exact timetable depends on the skills and desires of the successful candidate and upon the needs of the department. There is also the opportunity to do additional paid cross-sectional reporting sessions subject to demand.
Example Timetable:
Monday
Tuesday
Wednesday
Thursday
Friday
AM
Research
Research
MR
Supporting Activity
Research
PM
Supporting Activity
CT
Research
MR
CT
Weekend working will consist of clinical activities that are scheduled in advance and reviewed where required as work schedules are reviewed, taking account of service needs.
On call CommitmentsThis role does not currently require participation in the on-call rota. However, there is future potential for the introduction of cover for the on-call rota. This would not include night shifts.
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIESThe medical establishment consists of 27 Consultants, 3 Clinical Fellows in Oncology Imaging, 1 Clinical Fellow in Interventional Radiology and up to 5 Specialist Trainees in Clinical Radiology. The directorate also collaborates with 3 additional Consultants from other GM Trusts that support PET-CT reporting.
The Clinical Director has professional responsibility for medical staff and clinical responsibility for the Radiology service. They are supported by the Lead Consultants in CT, MR, US, Interventional Radiology, Nuclear Medicine, General Radiology, Clinical Audit and Information Technology and by the clinical tutors for the specialist trainees and fellows.
The appointee will be based at The Christie and will provide senior input to education and training in specialist cancer imaging, including sub-specialisms in CT and MR. The post holder will be supported in producing imaging reports and in further enhancing their involvement with specialist MDTs. Within Research they will lead project to evaluate the diagnostic accuracy, inter-observer reliability, and predictive value of a standardized CT-PCI atlas in patients with non-mucinous appendiceal adenocarcinoma.
The post holders routine clinical work will initially be closely supervised but they will practice increasingly independently as their experience develops during the year. In turn, the post holder will be able to supervise trainee Radiologists as time and expertise progress.
The significant proportion of time dedicated to research will be supported by dedicated research time by Dr Joe Mercer and Dr Rohit Kochhar, and the successful candidate is expected to contribute to projects leading to scientific publications, as well as presentations at national and international meetings.
Teaching Commitment:The department is active in teaching radiology trainees on the North-West training scheme, with further commitments to national and regional radiology teaching. Medical student, FY/CMT and non-radiology ST-teaching is also supported. The post holder will undertake lectures and tutorials to medical and non-medical staff in collaboration with and independent of colleagues.
Multi-Disciplinary Team Meetings:The Consultant Radiologists support the provision of around 25 separate MDT meetings. The post holder will be expected to participate in MDTs, with subspecialist interests accommodated.
Clinical Governance:The post-holder will be expected to participate in all relevant aspects of clinical governance, including maintaining and improving protocols, the consent process, discrepancy reporting, guidelines and clinical audit in conjunction with the other staff in the department. In addition, opportunities exist to be involved with national audit programs of the relevant specialist societies.
Office and Secretarial:The Trust will provide shared office space with other radiology trainees and fellows. Secretarial support is shared between consultants and trainees / fellows.
Continuing Professional DevelopmentThe Trust supports the requirements for continuing professional development (CPD) as laid down by the GMC and surgical colleges and is committed to providing time and financial support for these activities.
Role PlanningBoth part-time and full-time applications will be considered. The post will be offered as 40 hours per week, divided into 20 hours of direct clinical care, 16 hours dedicated research time and 4 hours of supporting activities; this will be reduced proportionally for part-time applications.An indicative timetable is described below (each session lasting 4 hours). Please note that an individualized timetable will be agreed with the Clinical Director, and the fellow supervisor. The exact timetable depends on the skills and desires of the successful candidate and upon the needs of the department. There is also the opportunity to do additional paid cross-sectional reporting sessions subject to demand.
Example Timetable:
Monday
Tuesday
Wednesday
Thursday
Friday
AM
Research
Research
MR
Supporting Activity
Research
PM
Supporting Activity
CT
Research
MR
CT
Weekend working will consist of clinical activities that are scheduled in advance and reviewed where required as work schedules are reviewed, taking account of service needs.
On call CommitmentsThis role does not currently require participation in the on-call rota. However, there is future potential for the introduction of cover for the on-call rota. This would not include night shifts.
Person Specification
Qualifications
Essential
- GMC registration
- FRCR
- Record of research
- ST in clinical radiology
- Medical Degree
Desirable
- Within 6 months CCST at time of appointment
- Recent publications in peer reviewed journals.
- Presentations at international meetings.
- Presentations at national meetings.
Experience
Essential
- Experience in specialist oncological radiology: cross-sectional imaging
- Record of audit
- Undergraduate and postgraduates resident radiologists
Desirable
- Clinical Audit design
PERSONAL SKILLS
Essential
- Flexible and team working
- Good leadership skills
- Resilient
- Motivated and Enthusiastic
- Reliable work record.
Desirable
- Multi-source feedback
Person Specification
Qualifications
Essential
- GMC registration
- FRCR
- Record of research
- ST in clinical radiology
- Medical Degree
Desirable
- Within 6 months CCST at time of appointment
- Recent publications in peer reviewed journals.
- Presentations at international meetings.
- Presentations at national meetings.
Experience
Essential
- Experience in specialist oncological radiology: cross-sectional imaging
- Record of audit
- Undergraduate and postgraduates resident radiologists
Desirable
- Clinical Audit design
PERSONAL SKILLS
Essential
- Flexible and team working
- Good leadership skills
- Resilient
- Motivated and Enthusiastic
- Reliable work record.
Desirable
- Multi-source feedback
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Radiology - E00298
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Radiology - E00298
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Consultant Medical Oncology - Colorectal Oncology
The Christie NHS FT View all jobs
Posted 1 month(s) ago
Reference: 413-MD-RR2026-000170-OO
Job summary
This post is for 8 Programmed Activities (PAs) per week to work within the Medical Oncology Colorectal Disease Group mainly based at The Christie site at Withington and one day based at Leighton.
Main duties of the job
The medical oncologist appointed will work with the colorectal team to provide a comprehensive clinical service for colorectal patients. This includes patients in the outpatient, inpatient and ambulatory settings, delivering Systemic Anti-Cancer Therapy (SACT) and providing Medical Oncology input to the Colorectal MDT including a clinic at Leighton.
Main Duties include:o Management of colorectal patients receiving standard & clinical trials including treatment decisions and ongoing care
o Participating in all relevant aspects of clinical governance, including maintaining up to date protocols, guidelines and clinical audit, under the supervision of the other consultants in the unit
o Contribute to current research projects and establish new opportunities to expand & develop research within the team
o Revision & development of evidence-based protocols for patients & undertaking the administrative duties associated with the care of their patients
o Maintaining a level of continuing professional development consistent the recommendations of the Royal College & Physicians
o Contributing to undergraduate teaching of medical students
o Actively contributing to the training of resident doctors & other multi-disciplinary team members in both in-patient & outpatient departments
o Undertake clinical audit as a member of The Christie Medical Staff Committee
o Participation in the Medical Oncology Consultant on call rota 1:20.
About us
The postholder will contribute to the delivery of high-quality consultant-led care across 7 days. This includes participation in planned weekend and weekday clinical activity to support safe, timely decision-making and continuity of care for patients.
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
28 August 2026
Pay scheme
Hospital medical and dental staff
Grade
Consultant
Salary
£113,565 to £150,569 a year Per Annum
Contract
Permanent
Working pattern
Part-time
Reference number
413-MD-RR2026-000170-OO
Job locations
Medical Oncology - E00251
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
Job Plan TimetableThe timetable below is indicative and will be confirmed on commencement in post.
It is the requirement of the Trust that all new consultant colleagues must have 0.25 SPAs within their job plan to support Trust appraisal and supervision requirements. This can either be as appraiser or a supervisor for medical staff or Advanced Clinical Practitioners (ACP).
Monday
Tuesday
Wednesday
Thursday
Friday
AM
Pelvic MDT (0.25PA)
LGI Clinic
(1PA)
Admin
(0.25PA)
Ward Round
(0.25PA)
SPA (0.5PA)
NWD
MDT
(0.25PA)
Leighton Clinic
(0.75PA)
LGI Radiology meeting
Immuno toxicity referral clinic (1PA)
PM
Admin (0.75PA)
SPA
(1PA)
NWD
Leighton
(1PA)
SPA
(1PA)
NB This timetable is indicative
Job Plan PA Summary
Total PAs Direct Clinical Care (DCC)5.5
Clinics
3.75
MDT
0.5
Ward Round
0.25
Admin
1.0
Supporting Professional Activities (SPA) (including 1.5 core SPA)
2.5
Supervision role (minimum 0.25 must be allocated)
0.25
SPA
2.25
Total Programmed Activities (PAs)
8
On call CommitmentsThis role does require participation in the on-call rota. This is a 1:20week rota and includes input to the acute admissions unit at the weekend.
Job description
Job responsibilities
Job Plan TimetableThe timetable below is indicative and will be confirmed on commencement in post.
It is the requirement of the Trust that all new consultant colleagues must have 0.25 SPAs within their job plan to support Trust appraisal and supervision requirements. This can either be as appraiser or a supervisor for medical staff or Advanced Clinical Practitioners (ACP).
Monday
Tuesday
Wednesday
Thursday
Friday
AM
Pelvic MDT (0.25PA)
LGI Clinic
(1PA)
Admin
(0.25PA)
Ward Round
(0.25PA)
SPA (0.5PA)
NWD
MDT
(0.25PA)
Leighton Clinic
(0.75PA)
LGI Radiology meeting
Immuno toxicity referral clinic (1PA)
PM
Admin (0.75PA)
SPA
(1PA)
NWD
Leighton
(1PA)
SPA
(1PA)
NB This timetable is indicative
Job Plan PA Summary
Total PAs Direct Clinical Care (DCC)5.5
Clinics
3.75
MDT
0.5
Ward Round
0.25
Admin
1.0
Supporting Professional Activities (SPA) (including 1.5 core SPA)
2.5
Supervision role (minimum 0.25 must be allocated)
0.25
SPA
2.25
Total Programmed Activities (PAs)
8
On call CommitmentsThis role does require participation in the on-call rota. This is a 1:20week rota and includes input to the acute admissions unit at the weekend.
Person Specification
Attainments
Essential
- MRCP or equivalent qualification
- GMC registration with a license to practice Entry on the General Medical Council (GMC) specialist register via one of the following: a.Certificate of Completion of Training (CCT) (the proposed CCT date must be within 6 months of interview) b.Certificate of Eligibility for Specialist Registration (CESR).
Desirable
- Evidence of productive research activity
Experience
Essential
- Advanced Trainee Competencies LGI Cancers and Acute oncology experience
- Active in local teaching
Desirable
- Productive engagement with clinical management/audit
- Active in national/international teaching education
Personal Skills
Essential
- Is a team player prepared to adapt to changing circumstances.
- Dynamic, decision-making motivator.
- Confident in ability but knowing own limitations.
- Hard working, enthusiastic achiever.
Person Specification
Attainments
Essential
- MRCP or equivalent qualification
- GMC registration with a license to practice Entry on the General Medical Council (GMC) specialist register via one of the following: a.Certificate of Completion of Training (CCT) (the proposed CCT date must be within 6 months of interview) b.Certificate of Eligibility for Specialist Registration (CESR).
Desirable
- Evidence of productive research activity
Experience
Essential
- Advanced Trainee Competencies LGI Cancers and Acute oncology experience
- Active in local teaching
Desirable
- Productive engagement with clinical management/audit
- Active in national/international teaching education
Personal Skills
Essential
- Is a team player prepared to adapt to changing circumstances.
- Dynamic, decision-making motivator.
- Confident in ability but knowing own limitations.
- Hard working, enthusiastic achiever.
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Medical Oncology - E00251
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Medical Oncology - E00251
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-109925-RI-RS
Job summary
We're looking for a full time Band 5 Clinical Research Practitioner to coordinate and deliver clinical research studies at The Christie NHS Foundation Trust. The successful candidate will either be a registered Clinical Research Practitioner with the Academy of Healthcare Sciences or working towards registration.
We are looking for a highly motivated and enthusiastic individual who can contribute to the development of clinical research for people with cancer within the Gynaecology Research Team.
We have an extensive portfolio of trials, NIHR academic and commercial clinical trials. The role of the CRP will involve recruiting patients to these clinical trials, obtaining informed consent where appropriate, supporting patients enrolled in clinical trials, and ensuring study interventions are completed according to Good Clinical Practice (GCP) and Trust standards.
You will be working within a supportive team of experienced clinical research nurses and the clinical trial administration team.
Main duties of the job
The post will involve coordinating a portfolio of research studies across different specialties within the Trust and is ideal for individuals with an interest in Gynaecology and experience of working in a busy clinical / research environment who wish to further develop their skills and experience.
We are seeking candidates with experience in working in clinical research in the NHS that can demonstrate knowledge of Good Clinical Practice and clinical skills, such as phlebotomy. Strong communication and organisational skills are essential, and a flexible working approach is a key element to this role.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
24 August 2026
Pay scheme
Agenda for change
Band
Band 5
Salary
£32,073 to £39,043 a year Per annum, Pro rata
Contract
Permanent
Working pattern
Full-time
Reference number
413-109925-RI-RS
Job locations
Gynae - Q00063
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIESThe specific responsibilities will depend on the requirements of each team, but mayinclude:Management Provide induction support and training to new and existing clinical trials staff, including development of training sessions and guidance documents. Encourage the sharing of best practice and dissemination of information through regular structured meetings with all trials administration staff. Assist with metric tracking for performance indicators including mandatory training requirements, divisional key performance indicators (i.e. time to recruitingfirst patient from NHS permission, patient recruitment to time and target), amendment timelines and divisional absences.Clinical Research Co-ordination/ Data Management Interview, recruit, take informed consent and support patients and carers in non treatment clinical trials/studies. This involves educating patients on the trials involved, explaining the advantages and disadvantages of taking part in non treatment trials, whilst remaining unbiased at all times. Assess patients as required by trial protocols. Maintain adequate patient records and ensure all relevant information is documented in the patients medical and nursing notes. Provide continuity of care for patients and their carers throughout the trial programme. Provide non-clinical advice and support as appropriate. Ensure the provision of optimal patient care by alerting appropriate clinical colleagues when referral to other members of the MDT may be required. Act as a key point of contact with the R&D core team, study sponsors, clinical research organisations and specific research teams. Co-ordinate feasibility activities for new studies under direction from Clinical research Nurse Team Leaders and Principal Investigators Manage the set up and initiation of allocated clinical trials within assigned Clinical research Teams. Understand and deliver protocols in accordance with regulatory requirements Financial management of study set-up costs and income recovery for assigned clinical trials in conjunction with the R&D Business Planning and Finance teams with oversight from the Clinical Research Nurse Team Leaders/ Senior Clinical Research Nurses. Oversee maintenance of investigator site files and essential documentation in accordance with ICH-GCP and Trust Standard Operating Procedures (SOPs) to ensure they are kept inspection ready at all times. Assist with preparation for audit and inspections within assigned teams and implementation of action plans. Understand the process for obtaining NHS permissions (R&D approval) for conducting clinical trials at site. As project lead, ensure permissions are in place prior to any patient recruitment. Ensure all clinical trial activities are recorded in appropriate systems in a timely manner. Awareness of trial specific, regional and national targets. Identify and implement strategies for recruiting patients to clinical trials ensuring that targets for patient recruitment are delivered. Arrange and facilitate clinical trial related meetings. Undertake general administrative tasks as delegated by managerial representatives from the R&D division to contribute to the smooth running of the patient recruitment teams. Implement and coordinate reporting mechanisms to ensure that research staff complete and return proformas containing up-dated information on patients included in the study. Oversee and complete case report forms and participate in monitoring visits as per sponsor requirements. Ensure that data is available and up to date for any meetings related to the trial/ study, producing minutes as required. Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team. Attend disease-specific research team meetings to maintain an overview of team activity. Ensure that all documents are archived in the appropriate way by following the Trusts archiving guidelines.
Clinical Service Responsibilities Demonstrate awareness of divisional and trust strategic objectives including performance indicators and metrics. Escalation of governance issues impacting on delivery of job purpose. To act as a primary contact point for the clinical trial patients for define clinical trials and act as adviser to other health care professionals. Participate in monitoring and audit activities within research team
PERSONAL AND PEOPLE DEVELOPMENT Maintain professional development whilst evaluating own specialist knowledge with assistance from their assigned line manager to satisfy the NHS Knowledge and Skills Framework. Participate in and deliver Trust-wide education programmes and study days, regional and national meetings and research seminars as appropriate.
PHYSICAL, MENTAL AND EMOTIONAL EFFORT Long periods of time spent using keyboard to input information and use of VDU for electronic communication. Prolonged concentration is regularly required (e.g. when checking through trial documentation and entering data into spreadsheets). Occasional exposure to distressed circumstances as trial patients are commonly suffering from terminal illnesses.
KEY VALUES Demonstrates the agreed set of values and accountable for own attitude and behaviour.
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIESThe specific responsibilities will depend on the requirements of each team, but mayinclude:Management Provide induction support and training to new and existing clinical trials staff, including development of training sessions and guidance documents. Encourage the sharing of best practice and dissemination of information through regular structured meetings with all trials administration staff. Assist with metric tracking for performance indicators including mandatory training requirements, divisional key performance indicators (i.e. time to recruitingfirst patient from NHS permission, patient recruitment to time and target), amendment timelines and divisional absences.Clinical Research Co-ordination/ Data Management Interview, recruit, take informed consent and support patients and carers in non treatment clinical trials/studies. This involves educating patients on the trials involved, explaining the advantages and disadvantages of taking part in non treatment trials, whilst remaining unbiased at all times. Assess patients as required by trial protocols. Maintain adequate patient records and ensure all relevant information is documented in the patients medical and nursing notes. Provide continuity of care for patients and their carers throughout the trial programme. Provide non-clinical advice and support as appropriate. Ensure the provision of optimal patient care by alerting appropriate clinical colleagues when referral to other members of the MDT may be required. Act as a key point of contact with the R&D core team, study sponsors, clinical research organisations and specific research teams. Co-ordinate feasibility activities for new studies under direction from Clinical research Nurse Team Leaders and Principal Investigators Manage the set up and initiation of allocated clinical trials within assigned Clinical research Teams. Understand and deliver protocols in accordance with regulatory requirements Financial management of study set-up costs and income recovery for assigned clinical trials in conjunction with the R&D Business Planning and Finance teams with oversight from the Clinical Research Nurse Team Leaders/ Senior Clinical Research Nurses. Oversee maintenance of investigator site files and essential documentation in accordance with ICH-GCP and Trust Standard Operating Procedures (SOPs) to ensure they are kept inspection ready at all times. Assist with preparation for audit and inspections within assigned teams and implementation of action plans. Understand the process for obtaining NHS permissions (R&D approval) for conducting clinical trials at site. As project lead, ensure permissions are in place prior to any patient recruitment. Ensure all clinical trial activities are recorded in appropriate systems in a timely manner. Awareness of trial specific, regional and national targets. Identify and implement strategies for recruiting patients to clinical trials ensuring that targets for patient recruitment are delivered. Arrange and facilitate clinical trial related meetings. Undertake general administrative tasks as delegated by managerial representatives from the R&D division to contribute to the smooth running of the patient recruitment teams. Implement and coordinate reporting mechanisms to ensure that research staff complete and return proformas containing up-dated information on patients included in the study. Oversee and complete case report forms and participate in monitoring visits as per sponsor requirements. Ensure that data is available and up to date for any meetings related to the trial/ study, producing minutes as required. Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team. Attend disease-specific research team meetings to maintain an overview of team activity. Ensure that all documents are archived in the appropriate way by following the Trusts archiving guidelines.
Clinical Service Responsibilities Demonstrate awareness of divisional and trust strategic objectives including performance indicators and metrics. Escalation of governance issues impacting on delivery of job purpose. To act as a primary contact point for the clinical trial patients for define clinical trials and act as adviser to other health care professionals. Participate in monitoring and audit activities within research team
PERSONAL AND PEOPLE DEVELOPMENT Maintain professional development whilst evaluating own specialist knowledge with assistance from their assigned line manager to satisfy the NHS Knowledge and Skills Framework. Participate in and deliver Trust-wide education programmes and study days, regional and national meetings and research seminars as appropriate.
PHYSICAL, MENTAL AND EMOTIONAL EFFORT Long periods of time spent using keyboard to input information and use of VDU for electronic communication. Prolonged concentration is regularly required (e.g. when checking through trial documentation and entering data into spreadsheets). Occasional exposure to distressed circumstances as trial patients are commonly suffering from terminal illnesses.
KEY VALUES Demonstrates the agreed set of values and accountable for own attitude and behaviour.
Person Specification
Qualifications
Essential
- Scientific Degree or relevant experience in scientific and medical research
Desirable
- Registered Clinical Research Practitioner with the Academy of Healthcare Sciences or working towards registration.
- Post Graduate certificate in Clinical Research or other relevant post graduate qualification/experience.
- Working knowledge of Microsoft Office (ECDL qualification or equivalent)
Experience
Essential
- Experience in clinical trials administration, data management involving clinical trials or project co-ordination
- Experience of working within a health care system and within a multidisciplinary clinical team
- NHS experience
Desirable
- Collection and processing of bloods
- Experience working in oncology
- Experience dealing with queries from patients and their families regarding sensitive issues
Skills
Essential
- Excellent organisational skills
- Excellent interpersonal skills
- Good oral and written Communication skills
- IT literate
- Attention to detail
Desirable
- Advanced use of spreadsheets
- Ability to create PowerPoint presentations and other Microsoft office applications
- Ability and willingness to train in clinical skills
Knowledge
Essential
- Understanding of clinical research
- GCP guidelines/EU directives
- Knowledge of clinical governance
- Knowledge of patient information systems
Desirable
- Knowledge of medical terminology
- Knowledge of oncology
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Tactful and diplomatic
- Flexible
- Conscientious and hardworking
- Ability to work unsupervised or as part of a team
- Ability to work to tight and/or unexpected deadlines
Desirable
- Evidence of CPD
- Evidence of achievement under pressure
Person Specification
Qualifications
Essential
- Scientific Degree or relevant experience in scientific and medical research
Desirable
- Registered Clinical Research Practitioner with the Academy of Healthcare Sciences or working towards registration.
- Post Graduate certificate in Clinical Research or other relevant post graduate qualification/experience.
- Working knowledge of Microsoft Office (ECDL qualification or equivalent)
Experience
Essential
- Experience in clinical trials administration, data management involving clinical trials or project co-ordination
- Experience of working within a health care system and within a multidisciplinary clinical team
- NHS experience
Desirable
- Collection and processing of bloods
- Experience working in oncology
- Experience dealing with queries from patients and their families regarding sensitive issues
Skills
Essential
- Excellent organisational skills
- Excellent interpersonal skills
- Good oral and written Communication skills
- IT literate
- Attention to detail
Desirable
- Advanced use of spreadsheets
- Ability to create PowerPoint presentations and other Microsoft office applications
- Ability and willingness to train in clinical skills
Knowledge
Essential
- Understanding of clinical research
- GCP guidelines/EU directives
- Knowledge of clinical governance
- Knowledge of patient information systems
Desirable
- Knowledge of medical terminology
- Knowledge of oncology
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Tactful and diplomatic
- Flexible
- Conscientious and hardworking
- Ability to work unsupervised or as part of a team
- Ability to work to tight and/or unexpected deadlines
Desirable
- Evidence of CPD
- Evidence of achievement under pressure
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
Gynae - Q00063
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Gynae - Q00063
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-108955-CMPE-DA
Job summary
We are looking for an enthusiastic and motivated Radiopharmaceutical Technologist with experience in aseptic dispensing to join our dynamic and expanding Radiopharmacy team. Experience of Radiopharmacy is desirable but full support and training will be provided to candidates who meet the other specifications.
Consideration would be given to a less experienced applicant to join the team as a trainee.
Main duties of the job
Applicants must have the ability to work in an aseptic unit under current GMP guidelines and local rules. The successful candidates will be responsible, under the supervision of the Production Manager, for the delivery of Radiopharmacy Aseptic Services, including participation in and supervising of aseptic dispensing and manufacturing activities. They would also participate in the quality control of the radiopharmaceuticals and contribute to the day to day running of the department in a proactive manner.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
21 August 2026
Pay scheme
Agenda for change
Band
Band 5
Salary
£32,073 to £39,043 a year Per annum, Pro rata
Contract
Permanent
Working pattern
Full-time
Reference number
413-108955-CMPE-DA
Job locations
CMPE RadioPharmacy - D00014
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
1. Regional Radiopharmacy
To be part of the team that carries out the daily production of radiopharmaceuticals within the Regional Radiopharmacy, in compliance with the requirements of The Human Medicine Regulations 2012, The Ionising Radiation (Medical Exposure) Regulations 2017 and amendment 2024, The Ionising Radiations Regulations 2017 and The Environmental Permitting Regulations. This includes:
1.1 Receipt of orders from customer departments1.2 Preparation of the Radiopharmacy prior to each production run1.3 Preparation of materials prior to Radiopharmacy production runs, including radionuclide generators1.4 Participation in the complex processes for production of Tc-99m labelled radiopharmaceuticals using aseptic techniques, and working with due speed and efficiency.1.5 Participation in the complex processes for production of Ga-68 and In-111 Octreoscan for same-day administration to Christie patients, using aseptic techniques1.6 Packaging and dispatch of QC products to other hospitals, including liaison with drivers1.7 Decontamination and cleaning of the Radiopharmacy post production, including tidying of waste and restocking of consumables1.8 Packaging and return of used radionuclide generators to manufacturers1.9 Production of the documentation for all the above processes (in compliance with GMP and data integrity principles)1.10 Proposes changes to policies and procedures1.11 Acts as in-process checking technician for the Radiopharmacy routine service and maintain this practice in accordance with local policy
2. Quality control
Carries out the programme of quality control of radiopharmaceuticals produced within the Regional Radiopharmacy, in compliance with the requirements of the Medicines Act. This includes:
2.1 Analysis of radiochemical purity using chromatography techniques (ITLC and HPLC)2.2 pH testing2.3 Radionuclidic purity testing2.4 Analysis of endotoxin levels2.5 Ensuring that working areas are cleared after each operation
3. Environmental and microbiological monitoring
Participates in the programme of environmental and microbiological monitoring of the Radiopharmacy and blood labelling suites, to include:
3.1 Air quality and air flows3.2 Microbiological contamination3.3 Periodic monitoring of aseptic compliance for each member of staff3.4 Integrity of air seals in the blood labelling suite
4. Regional blood cell labelling service
In the absence of the Senior Radiopharmaceutical Technologist, to be responsible on a day to day basis for the operation of the Regional blood cell labelling service, including:
4.1 Aseptic preparation of radio-labelled red and white blood cells, in multi-stage patient-critical procedures, prior to re-injection of the cells into patients for diagnostic scanning purposes4.2 Liaison with customer departments for scheduling, transportation of blood to and from the customer department, and other arrangements
5. Management, supervision and training of staff
5.1 Deputises for the Senior Radiopharmaceutical Technologist in their absence.
5.2 Assists in the training of new staff and supervises the work of more junior members of the department
6. Stock control
Responsible for stock control and ordering of pharmaceutical products, including:
6.1 Pharmaceutical products, chemical reagents, and disposable items used in the radiopharmacy and associated areas6.2 Consumable items for the Clinical Isotopes Department6.3 Orders stock items for Radiopharmacy and Clinical Isotopes from Pharmacy
7. Training
7.1 Assists in the training of junior Radiopharmacy staff7.2 Introduces pre-registration pharmacists and radiography students to Radiopharmacy.
8. Radiation protection
8.1 Monitors the radiopharmacy for radioactive contamination, and records results8.2 Assesses requirement for decontamination procedures, and carries these out if necessary
9. Professional
9.1 Where applicable maintain GPhC Registration, for which participation in a continuous professional development programme is compulsory9.2 Participate in an Annual Personal Development Review (PDR)9.3 Demonstrates the agreed set of values and accountable for own attitude and behaviour
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
1. Regional Radiopharmacy
To be part of the team that carries out the daily production of radiopharmaceuticals within the Regional Radiopharmacy, in compliance with the requirements of The Human Medicine Regulations 2012, The Ionising Radiation (Medical Exposure) Regulations 2017 and amendment 2024, The Ionising Radiations Regulations 2017 and The Environmental Permitting Regulations. This includes:
1.1 Receipt of orders from customer departments1.2 Preparation of the Radiopharmacy prior to each production run1.3 Preparation of materials prior to Radiopharmacy production runs, including radionuclide generators1.4 Participation in the complex processes for production of Tc-99m labelled radiopharmaceuticals using aseptic techniques, and working with due speed and efficiency.1.5 Participation in the complex processes for production of Ga-68 and In-111 Octreoscan for same-day administration to Christie patients, using aseptic techniques1.6 Packaging and dispatch of QC products to other hospitals, including liaison with drivers1.7 Decontamination and cleaning of the Radiopharmacy post production, including tidying of waste and restocking of consumables1.8 Packaging and return of used radionuclide generators to manufacturers1.9 Production of the documentation for all the above processes (in compliance with GMP and data integrity principles)1.10 Proposes changes to policies and procedures1.11 Acts as in-process checking technician for the Radiopharmacy routine service and maintain this practice in accordance with local policy
2. Quality control
Carries out the programme of quality control of radiopharmaceuticals produced within the Regional Radiopharmacy, in compliance with the requirements of the Medicines Act. This includes:
2.1 Analysis of radiochemical purity using chromatography techniques (ITLC and HPLC)2.2 pH testing2.3 Radionuclidic purity testing2.4 Analysis of endotoxin levels2.5 Ensuring that working areas are cleared after each operation
3. Environmental and microbiological monitoring
Participates in the programme of environmental and microbiological monitoring of the Radiopharmacy and blood labelling suites, to include:
3.1 Air quality and air flows3.2 Microbiological contamination3.3 Periodic monitoring of aseptic compliance for each member of staff3.4 Integrity of air seals in the blood labelling suite
4. Regional blood cell labelling service
In the absence of the Senior Radiopharmaceutical Technologist, to be responsible on a day to day basis for the operation of the Regional blood cell labelling service, including:
4.1 Aseptic preparation of radio-labelled red and white blood cells, in multi-stage patient-critical procedures, prior to re-injection of the cells into patients for diagnostic scanning purposes4.2 Liaison with customer departments for scheduling, transportation of blood to and from the customer department, and other arrangements
5. Management, supervision and training of staff
5.1 Deputises for the Senior Radiopharmaceutical Technologist in their absence.
5.2 Assists in the training of new staff and supervises the work of more junior members of the department
6. Stock control
Responsible for stock control and ordering of pharmaceutical products, including:
6.1 Pharmaceutical products, chemical reagents, and disposable items used in the radiopharmacy and associated areas6.2 Consumable items for the Clinical Isotopes Department6.3 Orders stock items for Radiopharmacy and Clinical Isotopes from Pharmacy
7. Training
7.1 Assists in the training of junior Radiopharmacy staff7.2 Introduces pre-registration pharmacists and radiography students to Radiopharmacy.
8. Radiation protection
8.1 Monitors the radiopharmacy for radioactive contamination, and records results8.2 Assesses requirement for decontamination procedures, and carries these out if necessary
9. Professional
9.1 Where applicable maintain GPhC Registration, for which participation in a continuous professional development programme is compulsory9.2 Participate in an Annual Personal Development Review (PDR)9.3 Demonstrates the agreed set of values and accountable for own attitude and behaviour
Person Specification
Qualifications
Essential
- BTec level 3 and NVQ level 3 in pharmacy services, Science Manufacturing Technicians level 3 or Science Degree
Desirable
- Second year student Pharmacy Technicians
- Senior ATO with dispensing experience
Experience
Essential
- Extensive experience of aseptic dispensing
Desirable
- Experience of Radiopharmacy dispensing
- Management/supervisory experience
Skills
Essential
- Good communication skills.
- Ability to work both within a team, and independently in complex multi-stage procedures.
- Ability to think quickly and change plans at short notice.
- Ability to keep accurate and legible written records.
- Ability to work safely, quickly and meticulously with good manipulative skills.
- Conscientious approach.
Desirable
- Computer literacy
Knowledge
Essential
- Principles and practice of aseptic production techniques.
Desirable
- Practical awareness of radiation protection principles.
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- 6.00-6:30am start each day
Person Specification
Qualifications
Essential
- BTec level 3 and NVQ level 3 in pharmacy services, Science Manufacturing Technicians level 3 or Science Degree
Desirable
- Second year student Pharmacy Technicians
- Senior ATO with dispensing experience
Experience
Essential
- Extensive experience of aseptic dispensing
Desirable
- Experience of Radiopharmacy dispensing
- Management/supervisory experience
Skills
Essential
- Good communication skills.
- Ability to work both within a team, and independently in complex multi-stage procedures.
- Ability to think quickly and change plans at short notice.
- Ability to keep accurate and legible written records.
- Ability to work safely, quickly and meticulously with good manipulative skills.
- Conscientious approach.
Desirable
- Computer literacy
Knowledge
Essential
- Principles and practice of aseptic production techniques.
Desirable
- Practical awareness of radiation protection principles.
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- 6.00-6:30am start each day
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
CMPE RadioPharmacy - D00014
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
CMPE RadioPharmacy - D00014
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
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Posted 1 month(s) ago
Reference: 413-109854-RI-DA
Job summary
This is an exciting opportunity to join the Advanced Immune and Cellular Therapy (AICT) Team at The Christie NHS Foundation Trust; an international leader in cancer research and development and the largest cancer treatment centre of its kind in Europe. This is a fixed-term maternity cover post.
We are seeking an enthusiastic, highly motivated and experienced individual who will be responsible for various aspects of clinical trial coordination including liaising with trial sponsors, monitors and the wider research community, maintaining essential documentation, managing the set-up of new studies and overseeing the day to day running of open studies.
The successful candidate will need to demonstrate a good understanding of the clinical trials process, Good Clinical Practice (GCP) and clinical governance, and be IT literate with previous experience of administrative work. We are looking for a candidate with good organisation and communication skills, who can work well both in a team and using their own initiative. The successful candidate will also demonstrate good leadership skills that promote an environment of quality and learning.
Main duties of the job
The focus of this role is to provide support to sustain and improve an excellent level of service provision from a trial site perspective for our research partners. In order to support the growth of the AICT research portfolio, the successful candidate will work closely with senior research and operational staff to provide management support across a portfolio of complex early phase clinical trials.
They will act as the key coordinator for the AICT Research Team, ensuring the provision of a high-quality, efficient and responsive administrative service to support the successful delivery of clinical trials throughout the study lifecycle, from study set-up through to study closure and archiving.
The post holder will coordinate and oversee the administrative delivery of assigned clinical trials, supporting workload allocation across the Clinical Trials Coordinators whilst providing day-to-day guidance and line management support as required.
Working in partnership with senior research management and the multidisciplinary clinical team, the post holder will support compliance with Trust policies, Good Clinical Practice (GCP), ICH-GCP and all other applicable regulatory requirements.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
21 August 2026
Pay scheme
Agenda for change
Band
Band 5
Salary
£32,073 to £39,043 a year Per annum, Pro rata
Contract
Fixed term
Duration
12 months
Working pattern
Full-time
Reference number
413-109854-RI-DA
Job locations
AICT - Q02054
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
TEAM SUPPORT
Responsible for supporting and supervising workload allocation/ monitoring across administrative team members, escalating issues as appropriate to senior managers. Provide support to senior managers with general Human Resource activities, including but not limited to recruitment and selection and line management of administrative team members as required. This will be in accordance with Trust policies. Provide induction support and training to new and existing clinical trials staff through one-to-one and group learning activities. Encourage the sharing of best practice and dissemination of information through regular structured meetings with all trials administration staff. Assist with data collection for divisional metrics reports of key performance indicators.
CLINICAL TRIALS CO-ORDINATION/ DATA MANAGEMENT:
The specific responsibilities will depend on the requirements of each team, but may include: Act as a key point of contact with the core Research and Development team, study sponsors, clinical research organisations and specific research teams. Support feasibility activities for new studies under direction from senior managers and Principal Investigators. Manage the set up and initiation of allocated clinical trials within assigned Clinical Research Teams. Provide support for study set up and initiation that has been delegated to Clinical Trials Coordinators, escalating any delays as appropriate. Support with negotiations of study set-up costs and income recovery for assigned clinical trials in conjunction with the Research Divisions Business Planning and Finance teams with oversight from senior managers. Oversee maintenance of investigator site files and essential documentation in accordance with ICH-GCP and Trust Standard Operating Procedures (SOPs) to ensure they are kept inspection ready at all times. Oversee and process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines, escalating any delays with the core Research and Development office as appropriate. To have the appropriate administrative processes in place to ensure, with the Clinical Research Team, that adverse event incidents and forms are completed, reported and followed up to resolution as the study protocol and regulations require. Implement and coordinate reporting mechanisms to ensure that research staff complete and return proformas containing up-dated information on patients included in the study. Oversee and complete case report forms and participate in monitoring visits as per sponsor requirements. Liaise with internal staff and external collaborators to resolve queries. Provide information for senior managers including (but not limited to) case report form completion timeliness, data locks, data backlogs, work allocations and patient recruitment. Ensure that data is available and up to date for any meetings related to the trial/ study, producing minutes as required. Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team. Attend disease-specific research team meetings to maintain an overview of team activity. Assist with preparation for audit and inspections within assigned teams and implementation of action plans. Ensure that all documents are archived in the appropriate way by following the Trusts archiving guidelines. Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment teams. Demonstrates the agreed set of values and accountable for own attitude and behaviour
WORKING PRACTICE
Work closely with the Senior Research Management Team to implement new SOPs and working procedures within designated teams. Be pro-active in providing feedback on working practices within the research team and suggest new ways of working. The post holder is expected to use initiative and be able to work independently without close supervision. They are also expected to plan and organise their own time and workload activity with prioritisation, referring to senior managers as necessary. The post holder is guided by relevant protocols and SOPs, and expected to exercise judgement outside these areas.
PERSONAL AND PEOPLE DEVELOPMENT Maintain professional development whilst evaluating own specialist knowledge with assistance from their assigned line manager to satisfy the NHS Knowledge and Skills Framework. Participate in and deliver Trust-wide education programmes and study days, regional and national meetings and research seminars as appropriate.
PHYSICAL, MENTAL AND EMOTIONAL EFFORT Long periods of time spent using keyboard to input information and use of VDU for electronic communication. Prolonged concentration is regularly required (e.g. when checking through trial documentation and entering data into spreadsheets). Occasional exposure to distressed circumstances as trial patients are commonly suffering from terminal illnesses.
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
TEAM SUPPORT
Responsible for supporting and supervising workload allocation/ monitoring across administrative team members, escalating issues as appropriate to senior managers. Provide support to senior managers with general Human Resource activities, including but not limited to recruitment and selection and line management of administrative team members as required. This will be in accordance with Trust policies. Provide induction support and training to new and existing clinical trials staff through one-to-one and group learning activities. Encourage the sharing of best practice and dissemination of information through regular structured meetings with all trials administration staff. Assist with data collection for divisional metrics reports of key performance indicators.
CLINICAL TRIALS CO-ORDINATION/ DATA MANAGEMENT:
The specific responsibilities will depend on the requirements of each team, but may include: Act as a key point of contact with the core Research and Development team, study sponsors, clinical research organisations and specific research teams. Support feasibility activities for new studies under direction from senior managers and Principal Investigators. Manage the set up and initiation of allocated clinical trials within assigned Clinical Research Teams. Provide support for study set up and initiation that has been delegated to Clinical Trials Coordinators, escalating any delays as appropriate. Support with negotiations of study set-up costs and income recovery for assigned clinical trials in conjunction with the Research Divisions Business Planning and Finance teams with oversight from senior managers. Oversee maintenance of investigator site files and essential documentation in accordance with ICH-GCP and Trust Standard Operating Procedures (SOPs) to ensure they are kept inspection ready at all times. Oversee and process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines, escalating any delays with the core Research and Development office as appropriate. To have the appropriate administrative processes in place to ensure, with the Clinical Research Team, that adverse event incidents and forms are completed, reported and followed up to resolution as the study protocol and regulations require. Implement and coordinate reporting mechanisms to ensure that research staff complete and return proformas containing up-dated information on patients included in the study. Oversee and complete case report forms and participate in monitoring visits as per sponsor requirements. Liaise with internal staff and external collaborators to resolve queries. Provide information for senior managers including (but not limited to) case report form completion timeliness, data locks, data backlogs, work allocations and patient recruitment. Ensure that data is available and up to date for any meetings related to the trial/ study, producing minutes as required. Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team. Attend disease-specific research team meetings to maintain an overview of team activity. Assist with preparation for audit and inspections within assigned teams and implementation of action plans. Ensure that all documents are archived in the appropriate way by following the Trusts archiving guidelines. Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment teams. Demonstrates the agreed set of values and accountable for own attitude and behaviour
WORKING PRACTICE
Work closely with the Senior Research Management Team to implement new SOPs and working procedures within designated teams. Be pro-active in providing feedback on working practices within the research team and suggest new ways of working. The post holder is expected to use initiative and be able to work independently without close supervision. They are also expected to plan and organise their own time and workload activity with prioritisation, referring to senior managers as necessary. The post holder is guided by relevant protocols and SOPs, and expected to exercise judgement outside these areas.
PERSONAL AND PEOPLE DEVELOPMENT Maintain professional development whilst evaluating own specialist knowledge with assistance from their assigned line manager to satisfy the NHS Knowledge and Skills Framework. Participate in and deliver Trust-wide education programmes and study days, regional and national meetings and research seminars as appropriate.
PHYSICAL, MENTAL AND EMOTIONAL EFFORT Long periods of time spent using keyboard to input information and use of VDU for electronic communication. Prolonged concentration is regularly required (e.g. when checking through trial documentation and entering data into spreadsheets). Occasional exposure to distressed circumstances as trial patients are commonly suffering from terminal illnesses.
Person Specification
Qualifications
Essential
- Degree in a science or health related discipline or Relevant experience in scientific and medical research.
Desirable
- Post graduate certificate in clinical research or other relevant post graduate qualification.
- In possession of or working towards an NHS leadership academy qualification
Experience
Essential
- Significant experience in clinical trial administration and clinical trial data management.
- Experience of mentoring junior staff.
Desirable
- Previous experience of working in the NHS or other healthcare system.
- Line management experience.
- Involvement in education and staff development
Skills
Essential
- Ability to prioritise own and others workload and practice effective time management.
- Excellent written communication skills.
- IT literate including good understanding and demonstrated use of the full Microsoft Office suite.
- Accuracy and attention to detail.
- Excellent interpersonal skills.
- Excellent oral communication skills.
Desirable
- Advanced use of spreadsheets.
Knowledge
Essential
- Good understanding of the clinical research delivery processes, related standards, governance and legislation.
Desirable
- Understanding of medical terminology and cancer.
- Understanding of case report forms.
- Knowledge of patient information systems.
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Ability to work to tight and/or unexpected deadlines.
- Flexible with ability to adapt to service requirements
- Conscientious and hardworking.
- Ability to work unsupervised or as part of a team.
- Tactful and diplomatic.
Desirable
- Evidence of achievement under pressure.
Person Specification
Qualifications
Essential
- Degree in a science or health related discipline or Relevant experience in scientific and medical research.
Desirable
- Post graduate certificate in clinical research or other relevant post graduate qualification.
- In possession of or working towards an NHS leadership academy qualification
Experience
Essential
- Significant experience in clinical trial administration and clinical trial data management.
- Experience of mentoring junior staff.
Desirable
- Previous experience of working in the NHS or other healthcare system.
- Line management experience.
- Involvement in education and staff development
Skills
Essential
- Ability to prioritise own and others workload and practice effective time management.
- Excellent written communication skills.
- IT literate including good understanding and demonstrated use of the full Microsoft Office suite.
- Accuracy and attention to detail.
- Excellent interpersonal skills.
- Excellent oral communication skills.
Desirable
- Advanced use of spreadsheets.
Knowledge
Essential
- Good understanding of the clinical research delivery processes, related standards, governance and legislation.
Desirable
- Understanding of medical terminology and cancer.
- Understanding of case report forms.
- Knowledge of patient information systems.
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Ability to work to tight and/or unexpected deadlines.
- Flexible with ability to adapt to service requirements
- Conscientious and hardworking.
- Ability to work unsupervised or as part of a team.
- Tactful and diplomatic.
Desirable
- Evidence of achievement under pressure.
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Christie NHS FT
Address
AICT - Q02054
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
AICT - Q02054
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-108084-CSSS-DA
Job summary
We have an exciting opportunity for an experienced and driven registered nurse to join our Specialist Nutrition Support Nurse team (band 6, 37.5hrs/week), as part of the Christie nutrition and dietetic team in our world class cancer centre, providing an opportunity to develop your practice within this specialist area of nursing.
If you are you passionate and have and interest or experience of working within in nutrition and/or oncology, and experience of varied feeding tubes, such as gastrostomies, nasogastric tubes, nasojejunal tubes and want to develop your skills further, then this is the post for you. The experienced and well-established team will support with competency and confidence development for this specialist role.
As a member of the Specialist Nutrition Support Nurse team, you will work closely with the dietetic team, and, as well as collaborate with the wider MDT and stake holders, to deliver high quality patient centred care for patients requiring artificial nutrition.
Main duties of the job
As a band 6 Specialist Nutrition Support Nurse you will work within the team to provide a specialist nutrition support nurse service for patients aimed at continually improving standards of care and facilitating a multidisciplinary team approach.
You will participate in the nurse management of patients receiving artificial nutrition support via enteral feeding, utilising both gastrostomies, jejunostomies, nasogastric and nasojejunal routes, as well as supporting patients through the HPN (Home Parenteral nutrition) referral process, and provision of venting gastrojejunostomy support for some of these patients.
Working with the team you will ensure the nutritional needs of patients are met, providing counselling, tube training, tube placement/replacement, follow-up/aftercare for patients receiving artificial nutrition support, this includes supporting the gastrostomy drop clinic in conjunction with the nursing team.
You will work alongside the specialist nutrition support nurse team in the development and delivery of education and training programmes for health care professionals in the Trust and at regional level on nursing related nutritional care.
You will be an active member of the wider Nutrition and Dietetic team, and an active role model for the service. Within this role you will work closely with the wider MDT and external agencies to ensure national nutritional performance and clinical standards are met.
Please see job description for full duties.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
21 August 2026
Pay scheme
Agenda for change
Band
Band 6
Salary
£39,959 to £48,117 a year Per annum, Pro rata
Contract
Permanent
Working pattern
Full-time
Reference number
413-108084-CSSS-DA
Job locations
Dietetic Nursing - E00975
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
Clinical1. To support the senior nutrition nurse and be responsible for own caseload providing an expert assessment plan and evaluation within the specialist area for enteral tubes2. To conduct regular ward visits to ensure compliance with nutritional standards and act as a resource for nutrition care planning and feeding tubes care delivery.3. To be involved in patient selection and education regarding enteral and parenteral nutrition support.4. To attend multidisciplinary / best interest meetings to discuss management of patients requiring enteral or parenteral nutrition at home.5. To maintain accurate, comprehensive and up to date documentation on the patient electronic system of individual patients in line with local and national standards and trust policy on confidentiality.6. To cover and support the organisation of home parenteral nutrition feed discharge patients as required alongside other nutrition nurse colleagues
Enteral7. To counsel and educate patients during the consent process for placement of enteral feeding tubes.8. To be competent to place nasogastric feeding tubes.9. To coordinate the gastrostomy service in collaboration with the senior nutrition nurse and interventional radiology team.10. To provide follow-up after interventional procedures for nutritional support and help with audit of outcome data.11. To be able to place secondary gastrostomy tube devices in hospital.12. To work alongside the dietitians and be involved in the setting up of a home enteral feed to ensure a safe and timely discharge.13. To educate and support the patient, carers, nursing staff and district nurses on the care of enteral feeding tubes before and after discharge.14. To work with the senior nutrition nurse to develop the nutritional nursing care service to patients in line with national standards.15. To work closely with the nutrition nurse teams, dietitians, nurse leaders and nurse clinicians to promote good practice and lead and support changes in practice16. To take an active role in audit and annually supporting the review of nursing guidelines, policies and patient information concerning enteral and parenteral nutrition in conjunction with the dietitians and senior nutrition nurse.
17. To identify clinical issues and incidents within the Trust that reduces the quality of care within the specialist service. Devise strategies to counter these to ensure the delivery of safe and effective care.18. To maintain patient data and statistics for service development19. To attend and participate in departmental, professional update meetings and trust nutrition related meetings.20. To be responsible for own clinical professional development (CPD) to maintain competency and to ensure best practice.21. Take an active part in professional networks to ensure the exchange of knowledge and ideas, both locally and nationally. Contribute to the development of national policy.22. In conjunction with the senior nutrition nurse provide specialist nursing knowledge of nutritional care to medical and nursing staff and students23. In conjunction with the senior nutrition nurse deliver an education programme on the nurse management of oncology patients receiving nutrition support internally and externally at regional level to nursing staff and other health care professionals.24. To work with the senior nutrition nurse to develop the nutrition link nurse group and be accountable to the Nutrition steering group.25. To promote good nursing practice in enteral and parenteral feeding to ward staff.26. To participate in the education of nursing staff on nutritionally screening patients, care planning and protected mealtimes and carry out regular audits.
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
Clinical1. To support the senior nutrition nurse and be responsible for own caseload providing an expert assessment plan and evaluation within the specialist area for enteral tubes2. To conduct regular ward visits to ensure compliance with nutritional standards and act as a resource for nutrition care planning and feeding tubes care delivery.3. To be involved in patient selection and education regarding enteral and parenteral nutrition support.4. To attend multidisciplinary / best interest meetings to discuss management of patients requiring enteral or parenteral nutrition at home.5. To maintain accurate, comprehensive and up to date documentation on the patient electronic system of individual patients in line with local and national standards and trust policy on confidentiality.6. To cover and support the organisation of home parenteral nutrition feed discharge patients as required alongside other nutrition nurse colleagues
Enteral7. To counsel and educate patients during the consent process for placement of enteral feeding tubes.8. To be competent to place nasogastric feeding tubes.9. To coordinate the gastrostomy service in collaboration with the senior nutrition nurse and interventional radiology team.10. To provide follow-up after interventional procedures for nutritional support and help with audit of outcome data.11. To be able to place secondary gastrostomy tube devices in hospital.12. To work alongside the dietitians and be involved in the setting up of a home enteral feed to ensure a safe and timely discharge.13. To educate and support the patient, carers, nursing staff and district nurses on the care of enteral feeding tubes before and after discharge.14. To work with the senior nutrition nurse to develop the nutritional nursing care service to patients in line with national standards.15. To work closely with the nutrition nurse teams, dietitians, nurse leaders and nurse clinicians to promote good practice and lead and support changes in practice16. To take an active role in audit and annually supporting the review of nursing guidelines, policies and patient information concerning enteral and parenteral nutrition in conjunction with the dietitians and senior nutrition nurse.
17. To identify clinical issues and incidents within the Trust that reduces the quality of care within the specialist service. Devise strategies to counter these to ensure the delivery of safe and effective care.18. To maintain patient data and statistics for service development19. To attend and participate in departmental, professional update meetings and trust nutrition related meetings.20. To be responsible for own clinical professional development (CPD) to maintain competency and to ensure best practice.21. Take an active part in professional networks to ensure the exchange of knowledge and ideas, both locally and nationally. Contribute to the development of national policy.22. In conjunction with the senior nutrition nurse provide specialist nursing knowledge of nutritional care to medical and nursing staff and students23. In conjunction with the senior nutrition nurse deliver an education programme on the nurse management of oncology patients receiving nutrition support internally and externally at regional level to nursing staff and other health care professionals.24. To work with the senior nutrition nurse to develop the nutrition link nurse group and be accountable to the Nutrition steering group.25. To promote good nursing practice in enteral and parenteral feeding to ward staff.26. To participate in the education of nursing staff on nutritionally screening patients, care planning and protected mealtimes and carry out regular audits.
Person Specification
Qualifications
Essential
- Current NMC registration
- Diploma or degree in nursing studies
Desirable
- Mentorship module
Experience
Essential
- Experience in an acute setting NHS experience
- Experience in oncology
- Evidence of clinical audit
- Evidence of educational study in nutrition
- Evidence of interest in nutrition
- Evidence in recent management and care of patients with feeding tubes
Desirable
- Evidence of setting standards and producing action plans
- Experience in endoscopic / radiological procedures
- Experience in gastroenterology
Skills
Essential
- Able to deliver a high standard of evidence based individual patient care
- To provide all nursing care in line with Trust policies and protocols
- Good interpersonal skills and initiative.
- Able to work as part of a team Independently insert nasogastric tube
- Ability to train patients/carers for enteral tube care
- Assess gastrostomy tubes
- Provide aftercare for feeding tubes
- Able to teach formally and informally
- Able to present information written and verbal
- Computer literate
Desirable
- Replace gastrostomy tubes
Knowledge
Essential
- Up to date knowledge of nursing issues in relation to nutritional support, enteral feeding and parenteral feeding
- Understanding of national nutrition standards and guidelines (CQC, NPSA, PLACE, NICE)
- Knowledge of endoscopic and radiologic procedures for nutritional support
- Evidence of own personal continuing professional development (CPD)
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Able to work as autonomous practitioner
- Able to manage own workload
Person Specification
Qualifications
Essential
- Current NMC registration
- Diploma or degree in nursing studies
Desirable
- Mentorship module
Experience
Essential
- Experience in an acute setting NHS experience
- Experience in oncology
- Evidence of clinical audit
- Evidence of educational study in nutrition
- Evidence of interest in nutrition
- Evidence in recent management and care of patients with feeding tubes
Desirable
- Evidence of setting standards and producing action plans
- Experience in endoscopic / radiological procedures
- Experience in gastroenterology
Skills
Essential
- Able to deliver a high standard of evidence based individual patient care
- To provide all nursing care in line with Trust policies and protocols
- Good interpersonal skills and initiative.
- Able to work as part of a team Independently insert nasogastric tube
- Ability to train patients/carers for enteral tube care
- Assess gastrostomy tubes
- Provide aftercare for feeding tubes
- Able to teach formally and informally
- Able to present information written and verbal
- Computer literate
Desirable
- Replace gastrostomy tubes
Knowledge
Essential
- Up to date knowledge of nursing issues in relation to nutritional support, enteral feeding and parenteral feeding
- Understanding of national nutrition standards and guidelines (CQC, NPSA, PLACE, NICE)
- Knowledge of endoscopic and radiologic procedures for nutritional support
- Evidence of own personal continuing professional development (CPD)
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Able to work as autonomous practitioner
- Able to manage own workload
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Employer details
Employer name
The Christie NHS FT
Address
Dietetic Nursing - E00975
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Dietetic Nursing - E00975
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
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Posted 1 month(s) ago
Reference: 413-109617-RI-TM-DA
Job summary
We are seeking a Sponsorship Governance Facilitator to join the Sponsorship Team within the R&I Office at the Christie NHS Foundation Trust.
This is fantastic opportunity for an individual with clinical research management experience looking to take on a research governance role.
The post holder will provide advice and regulatory support to researchers from confirmation of grant application, through sponsorship and regulatory approval, initiation at sites, study conduct and close-down; ensuring studies meet regulatory requirements and other obligations as Sponsor, and working closely with investigators, project managers, internal research support services and external collaborating organisations throughout the lifecycle of a research study.
The study portfolio will include CTIMPs, device trials, surgical and interventional trials, basic science studies involving procedures with human participants, observational studies, qualitative research and studies working with tissue or data. The post holder will be required to work autonomously, managing their day-to-day workload and prioritising as needed.
Main duties of the job
As a key member of the sponsor team, you will provide regulatory support and advice to researchers and collaborators throughout the lifecycle of a portfolio of research studies, supporting the Trust to meet its obligations as research sponsor.
Ensuring a risk-based and collaborative approach you will provide ongoing oversight of study progress and key performance indicators to ensure that studies within the portfolio meet key milestones and all regulatory reporting requirements.
You will be required to liaise with external collaborators funding agencies (including industry, charities, Department of Health & Social Care, NIHR), and other organisations and Trust departments as required.
The ideal candidate will be proactive, highly organised and proficient in communicating with a wide range of stakeholders, as well as having the ability to navigate complex and competing priorities.
This post holder will have a strong understanding of standards and legislation that govern research practice in the NHS.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
20 August 2026
Pay scheme
Agenda for change
Band
Band 6
Salary
£39,959 to £48,117 a year Pro Rata Per Annum
Contract
Fixed term
Duration
12 months
Working pattern
Full-time
Reference number
413-109617-RI-TM-DA
Job locations
R&D Office - Q01552
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
Governance and Management
To be a sponsorship specialist for an allocated portfolio of Trust research studies and as such have significant discretion and freedom to act.
Provide guidance to investigators on the requirements for Christie sponsorship.
Advise and support investigators and Research Managers in ensuring appropriate costings are included in studies; to provide resource for sponsorship responsibilities at the grant application stage of agreeing provisional sponsorship or when initially presented with an internally funded study.
Support investigators with compiling documentation for regulatory submissions; Health Research Authority (HRA) including HRA assessment, Medicines and Healthcare products Regulatory Agency (MHRA) and Research Ethics Committee (REC), Confidentiality Advisory Group (CAG) and site requirements by advising and reviewing documentation.
Review all study related documentation to ensure it is of high standard, consistent with current regulatory requirements and advisory guidance and meets Trust sponsor obligations such as adequate peer review, risk assessment and data management. Ensuring data management plans are in place and that assurances are obtained to verify that the databases are fit for purpose.
Ensure the provision of Investigational Medicinal Product (IMP), placebo or devices as appropriate from approved providers to cover the duration of the trial.
Collaborate with the contracts team to assess and advise on contracts required and provide template documents for the necessary contractual requirements of the study. Review responsibilities, liaise with third parties as required and obtain appropriate authorisations for contracts, sponsorship agreements and study vendors.
Conduct sponsor review of study amendments, ensuring implications are assessed communication and functional areas involved as necessary prior to and changes being actioned.
Implement and follow sponsorship related SOPs.
Contribute to the development maintenance of sponsorship related SOPs and ensure their compliance with regulatory and Trust requirements. Implement changes to policy, and relevant SOPs, when national guidance changes within the sponsorship arena.
To contribute and assist in the preparation for external audit, monitoring and regulatory inspection by external agencies such as the MHRA.
Co-ordinating remedial action and ensuring completion of tasks in relation to CAPA planned following monitoring, audit. Inspection or incident/deviation related issues.
Portfolio OversightWork within sponsorship team to ensure routine processes implemented to meet sponsor obligations during study set-up, green-light (including other sites), regulatory reporting (e.g. progress reports and end of study reports), study closure and study results and publications.
Work to ensure activities are well planned and organised and tracked due to the varied nature of specific studies and the unpredictable workload involved.
Provide oversight of the management of Trust sponsored studies. Ensuring Trial Management Group meetings take place and attend where required, ensuring Trial Steering Committees and Data Management Committees are in place as required. Ensuring Clinical Trials Units, or other vendors, undertake their delegated contractual duties appropriately and in a timely fashion. Ensure Study Initiation Visits (SIVs) have taken place when required.
Receive and review progress reports as determined by the study risk management plan escalating any concerns as necessary.
Manage to resolution issues identified through the Trust monitoring and audit programme, which are the sponsors responsibility to action and oversee.
Information ManagementMaintain precise and accurate records that document the decisions made on behalf of the sponsor for the lifetime of the study.
Responsible for the operation of sponsor information systems (project planning tools and trackers) managing and maintaining the data within and developing where required for the Trust.
FinanceContribute to the oversight of study budgets by working with the R&I grants and income and costing functions.
Work with project teams and cross functional teams to ensure that study budgets are reconciled in a timely manner at the end of the study.
CommunicationEngage actively with investigators, academic collaborators, clinical research fellows, nurses, support departments, academic departments and external organisations to ensure they receive appropriate and tailored support.
Ensure all stakeholders are informed and involved at every level of sponsorship reviews.
Provide investigators with the necessary information on NIHR, HRA, MHRA and Trust processes. This may include multidisciplinary meetings, website and producing and maintaining other information materials.
Answer queries relating to legislation and the conduct of research from research staff promptly and efficiently. This information may be complex in nature, so good communication skills are required to make the information understandable to varying levels of staff. Acknowledging all communication from investigators and key stakeholders and ensuring an efficient flow of information.
Ensure there is good internal communication, with members of R&I infrastructure staff, of decision making and sponsorship pathway progress. Tact and sensitivity will need to be used when delivering negative news to recipients.
When communicating with external organisations, such as CTUs or other vendors, professionalism, persuasion, negotiation and assertiveness will be required to ensure the Trust receives the services required. There may also be a need to discuss shortcomings of the service being delivered where necessary in conjunction with other members of the R&I team.
Human Resources ManagementProvide effective leadership on sponsorship matters and know when to escalate to sponsorship manager.
Participate in recruitment of staff to the R&I central office and act as supervisor/mentor as required.
Job description
Job responsibilities
Governance and Management
To be a sponsorship specialist for an allocated portfolio of Trust research studies and as such have significant discretion and freedom to act.
Provide guidance to investigators on the requirements for Christie sponsorship.
Advise and support investigators and Research Managers in ensuring appropriate costings are included in studies; to provide resource for sponsorship responsibilities at the grant application stage of agreeing provisional sponsorship or when initially presented with an internally funded study.
Support investigators with compiling documentation for regulatory submissions; Health Research Authority (HRA) including HRA assessment, Medicines and Healthcare products Regulatory Agency (MHRA) and Research Ethics Committee (REC), Confidentiality Advisory Group (CAG) and site requirements by advising and reviewing documentation.
Review all study related documentation to ensure it is of high standard, consistent with current regulatory requirements and advisory guidance and meets Trust sponsor obligations such as adequate peer review, risk assessment and data management. Ensuring data management plans are in place and that assurances are obtained to verify that the databases are fit for purpose.
Ensure the provision of Investigational Medicinal Product (IMP), placebo or devices as appropriate from approved providers to cover the duration of the trial.
Collaborate with the contracts team to assess and advise on contracts required and provide template documents for the necessary contractual requirements of the study. Review responsibilities, liaise with third parties as required and obtain appropriate authorisations for contracts, sponsorship agreements and study vendors.
Conduct sponsor review of study amendments, ensuring implications are assessed communication and functional areas involved as necessary prior to and changes being actioned.
Implement and follow sponsorship related SOPs.
Contribute to the development maintenance of sponsorship related SOPs and ensure their compliance with regulatory and Trust requirements. Implement changes to policy, and relevant SOPs, when national guidance changes within the sponsorship arena.
To contribute and assist in the preparation for external audit, monitoring and regulatory inspection by external agencies such as the MHRA.
Co-ordinating remedial action and ensuring completion of tasks in relation to CAPA planned following monitoring, audit. Inspection or incident/deviation related issues.
Portfolio OversightWork within sponsorship team to ensure routine processes implemented to meet sponsor obligations during study set-up, green-light (including other sites), regulatory reporting (e.g. progress reports and end of study reports), study closure and study results and publications.
Work to ensure activities are well planned and organised and tracked due to the varied nature of specific studies and the unpredictable workload involved.
Provide oversight of the management of Trust sponsored studies. Ensuring Trial Management Group meetings take place and attend where required, ensuring Trial Steering Committees and Data Management Committees are in place as required. Ensuring Clinical Trials Units, or other vendors, undertake their delegated contractual duties appropriately and in a timely fashion. Ensure Study Initiation Visits (SIVs) have taken place when required.
Receive and review progress reports as determined by the study risk management plan escalating any concerns as necessary.
Manage to resolution issues identified through the Trust monitoring and audit programme, which are the sponsors responsibility to action and oversee.
Information ManagementMaintain precise and accurate records that document the decisions made on behalf of the sponsor for the lifetime of the study.
Responsible for the operation of sponsor information systems (project planning tools and trackers) managing and maintaining the data within and developing where required for the Trust.
FinanceContribute to the oversight of study budgets by working with the R&I grants and income and costing functions.
Work with project teams and cross functional teams to ensure that study budgets are reconciled in a timely manner at the end of the study.
CommunicationEngage actively with investigators, academic collaborators, clinical research fellows, nurses, support departments, academic departments and external organisations to ensure they receive appropriate and tailored support.
Ensure all stakeholders are informed and involved at every level of sponsorship reviews.
Provide investigators with the necessary information on NIHR, HRA, MHRA and Trust processes. This may include multidisciplinary meetings, website and producing and maintaining other information materials.
Answer queries relating to legislation and the conduct of research from research staff promptly and efficiently. This information may be complex in nature, so good communication skills are required to make the information understandable to varying levels of staff. Acknowledging all communication from investigators and key stakeholders and ensuring an efficient flow of information.
Ensure there is good internal communication, with members of R&I infrastructure staff, of decision making and sponsorship pathway progress. Tact and sensitivity will need to be used when delivering negative news to recipients.
When communicating with external organisations, such as CTUs or other vendors, professionalism, persuasion, negotiation and assertiveness will be required to ensure the Trust receives the services required. There may also be a need to discuss shortcomings of the service being delivered where necessary in conjunction with other members of the R&I team.
Human Resources ManagementProvide effective leadership on sponsorship matters and know when to escalate to sponsorship manager.
Participate in recruitment of staff to the R&I central office and act as supervisor/mentor as required.
Person Specification
Qualifications
Essential
- Post graduate diploma level in a scientific discipline or equivalent experience
Desirable
- Evidence of continuing professional development
Experience
Essential
- Previous experience of working within clinical research setting
- Experience of writing procedural/patient documentation
- Experience of working to deadlines
Skills
Essential
- Ability to assess and interpret complicated and conflicting information and use judgement where appropriate
- Ability to listen to others and use critical questioning techniques to identify core issues/risks within proposals
- Organisational and time management skills
- Interpersonal skills- Good written and oral communication skills
- Ability to work under pressure to tight timelines
Desirable
- Ability to use spreadsheets
- Ability to create PowerPoint presentations and other Microsoft office applications
- Advanced computer literacy and ability to adapt and learn new computer applications
Knowledge
Essential
- Knowledge of research sponsorship responsibilities
- Comprehensive knowledge and understanding of standards and legislation that govern research practice in the NHS.
- Comprehensive knowledge and understanding of NHS research governance processes, including amendments
- Knowledge of regulatory issues surrounding the conduct of clinical research
- Awareness of research within the NHS and legislative framework within the UK
Desirable
- Knowledge of quantitative and qualitative research methodologies
- Understanding of clinical trial protocol requirements
- Understanding of study data management systems.
- Knowledge of international research, and conduct.
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Able to work and act independently
- Ability to work across functional and organisational boundaries
- Good attention to detail
- Positive approach
- Flexible and motivated team player
Person Specification
Qualifications
Essential
- Post graduate diploma level in a scientific discipline or equivalent experience
Desirable
- Evidence of continuing professional development
Experience
Essential
- Previous experience of working within clinical research setting
- Experience of writing procedural/patient documentation
- Experience of working to deadlines
Skills
Essential
- Ability to assess and interpret complicated and conflicting information and use judgement where appropriate
- Ability to listen to others and use critical questioning techniques to identify core issues/risks within proposals
- Organisational and time management skills
- Interpersonal skills- Good written and oral communication skills
- Ability to work under pressure to tight timelines
Desirable
- Ability to use spreadsheets
- Ability to create PowerPoint presentations and other Microsoft office applications
- Advanced computer literacy and ability to adapt and learn new computer applications
Knowledge
Essential
- Knowledge of research sponsorship responsibilities
- Comprehensive knowledge and understanding of standards and legislation that govern research practice in the NHS.
- Comprehensive knowledge and understanding of NHS research governance processes, including amendments
- Knowledge of regulatory issues surrounding the conduct of clinical research
- Awareness of research within the NHS and legislative framework within the UK
Desirable
- Knowledge of quantitative and qualitative research methodologies
- Understanding of clinical trial protocol requirements
- Understanding of study data management systems.
- Knowledge of international research, and conduct.
Values
Essential
- Ability to demonstrate the organisational values and behaviours
Other
Essential
- Able to work and act independently
- Ability to work across functional and organisational boundaries
- Good attention to detail
- Positive approach
- Flexible and motivated team player
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
Employer details
Employer name
The Christie NHS FT
Address
R&D Office - Q01552
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
R&D Office - Q01552
Manchester
M20 4BX
United Kingdom
Employer's website
Apply Now
Already registered?
Sign in to pre-fill your personal details, attachments and more.
Success!
Your application has been submitted.
Posted 1 month(s) ago
Reference: 413-110169-CNS-DA
Job summary
Pharmacy technicians from community, prison, PCNs or other settings, are encouraged to apply. To arrange an informal visit or discuss the role and meet the team, please contact. Melanie Lowe, [email protected], 0161 918 2456 or 07526557349.
Are you confident, forward-thinking, and looking for a new challenge? Why not consider joining our clinical pharmacy team? You will be front and centre, talking with patients across our wards/departments, giving you a great opportunity to be a part of the delivery of treatments in oncology.
We are currently looking to recruit highly motivated, enthusiastic pharmacy technicians to join our Trust pharmacy team to work alongside a multi-disciplinary team in providing a high-quality service to patients and colleagues.
Part time and job share will be considered. The role involves weekend and bank holiday working on a rotational basis.
Working with us gives you the knowledge and sense of pride that every activity you do genuinely does make a difference to support our patients and staff, ensuring we keep thriving and delivering outstanding healthcare right across the organisation.You will have access to varied development opportunities, learn new skills, meet wonderful people, and do things you may never have done.
Main duties of the job
You will work closely with other members of our multi-disciplinary teams to ensure that Christie patients have access to the very latest developments in oncology and haematology medicines. You will be responsible for pharmacy technician clinical pharmacy services on designated wards, working within our innovative clinical pharmacy team to ensure a high quality, patient-focused clinical pharmacy and medicines supply service to oncology patients which will help you to enhance your skills, knowledge, and experience to support your future career development. You will support the satellite dispensary when required, including dispensing and accuracy checking of medication and facilitating medication requirements for chemotherapy patients on Oak Road Treatment Centre and haematology day case units. Other responsibilities within this role include controlled drug destruction, monitoring and replenishment of pharmacy resuscitation boxes and support within the Homecare service.
You will be a strong team player with effective interpersonal, communication and organisational skills as well as a keen interest and enthusiasm for patient focussed services and continual improvement.
The post holder will be based at the Christie Withington site, however, may be required to undertake roles and responsibilities at other 'Christie at' sites.
About us
The Christie is one of Europe's leading cancer centres, looking after more than 64,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 25% patients are referred to us from other parts of the country.
We are the largest radiotherapy provider in the NHS with one in 20 treatments delivered at The Christie. We have up to 15 linear accelerators operating across our network of sites. We operate the largest chemotherapy unit in the UK on our main site and treatments are also provided at 13 other networked sites, and in patients homes. And as a specialist tertiary surgical centre, we focus on rare cancers, complex procedures, and multidisciplinary approaches to cancer surgery, specialising in colorectal, peritoneal, gynaecological, urological and plastic surgery.
We are also an international leader in research, with world first breakthroughs for over 100 years. We have been named by the UK's National Institute for Health Research (NIHR), as one of the best hospitals providing opportunities for patients to participate in clinical research studies, with more than 800 studies open at any time, caring for over 3,000 patients.
Details
Date posted
20 August 2026
Pay scheme
Agenda for change
Band
Band 5
Salary
£32,073 to £39,043 a year Per annum, Pro rata
Contract
Permanent
Working pattern
Full-time
Reference number
413-110169-CNS-DA
Job locations
Pharmacy Clinical - E00920
Manchester
M20 4BX
United Kingdom
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
To participate, and be responsible for, pharmacy technician based clinical pharmacy services on designated wards in partnership with the ward pharmacist to ensure a high quality, patientfocused clinical pharmacy and medicines supply service to oncology patients is delivered. o To contribute to the service delivery within the day case units including oncology solid tumours, haematology, and ambulatory care initiatives.o To ensure each patient is assessed on admission regarding medicines management, taking a complete and accurate medication history.o Rotation onto the Acute Assessment Unit providing a medicines optimisation role.o To participate in the assessment of patients for the self-medication scheme in accordance with local policy.o To provide a weekly top up service for patients on designated wards to ensure continuous supply of medication.o To be responsible and assist the ward pharmacist in ensuring and organising the efficient supply of medication during the patients stay in hospital and on discharge from the hospital including assessing suitability of medication for discharge.o To be proactive in the discharge planning process and liaise with the ward pharmacist and other healthcare professionals to ensure prescriptions are processed and delivered to the patients in a timely manner.o To counsel patients and their carers to ensure greater understanding of their medication including its safe use and side effects.
To undertake all clinical duties in accordance with standard operating procedure and all local, Trust and national guidelines. Ensure good team working and communication between pharmacy staff, ward pharmacist, ward staff and medical staff on behalf of the patients. To deal with queries from patients and all healthcare professionals in a friendly and courteous manner. To assist in maintaining optimal stock levels of medication on all ward areas. To participate in the training and supervision of pharmacy assistants in the ordering, maintenance, and delivery of stock for wards and departments within the Trust. To assist in the training, induction and supervision of staff involved in ward-based technician services including pre-registration trainee pharmacy technicians, pharmacy technicians, pharmacy assistants, pre-registration pharmacists and new members of staff. To complete yearly Personal Development Reviews for staff including pre-registration trainee pharmacy technicians, pharmacy technicians and pharmacy assistants. To provide pharmacy technician cover at Christie @ sites as required. To contribute to the regular review and development of the clinical service. To demonstrate awareness and commitment to the Trusts Clinical & Research Governance agenda and to implement agreed clinical & research governance initiatives. To participate in departmental, Trust and National risk management schemes such as error reporting systems and intervention monitoring. To assist in clinical audit or practice research as required. To provide annual leave/absence cover for other clinical pharmacy technicians in their duties. To undertake general dispensary duties in accordance with standard operating procedures in line with the clinical needs of ward patients. To participate in the development of the satellite pharmacy service on Oak Road Treatment Centre. To support the satellite dispensary when required and facilitate the medication requirements for chemotherapy patients. To provide dispensing and accuracy checking duties within the satellite pharmacy. To coordinate medication requirements for haematology and ambulatory care day case units. To support the monitoring and replenishment of the resuscitation boxes within the Trust. To support the cyclical medication and homecare services when required. To support the Christie at Home service when required. To participate in controlled drug destruction in line with relevant SOPs and national guidance. To contribute to any investigation at ward level regarding anomalies or discrepancies with controlled drug stock or patients own controlled drugs, stored on the ward/department or any other medication related incidents as appropriate. To liaise with the Chief Clinical Pharmacy Technician when further investigation is required regarding controlled drug incidents or any other medication related incidents if the initial investigation is not resolved. To be an accredited accuracy checking technician and to support the satellite dispensary as required. To be fully aware of the COSHH regulations particularly regarding the safe storage and handling of pharmaceutical products. To participate in Continuing Professional Development ensuring relevant knowledge and skills are up to date, meeting the professional requirements of the General Pharmaceutical Council. To participate in mandatory training in line with Trust and departmental requirements. To participate in all department rotas including the extended opening hours of the department rota, weekend service (Saturdays and Sundays) and Bank Holiday working as requested. To always behave in a manner that is in accordance with the professional standards set by the General Pharmaceutical Council. Undertake all other related duties which may be required in accordance with the changing needs and practices of the department and organisation.
Job description
Job responsibilities
DUTIES AND RESPONSIBILITIES
To participate, and be responsible for, pharmacy technician based clinical pharmacy services on designated wards in partnership with the ward pharmacist to ensure a high quality, patientfocused clinical pharmacy and medicines supply service to oncology patients is delivered. o To contribute to the service delivery within the day case units including oncology solid tumours, haematology, and ambulatory care initiatives.o To ensure each patient is assessed on admission regarding medicines management, taking a complete and accurate medication history.o Rotation onto the Acute Assessment Unit providing a medicines optimisation role.o To participate in the assessment of patients for the self-medication scheme in accordance with local policy.o To provide a weekly top up service for patients on designated wards to ensure continuous supply of medication.o To be responsible and assist the ward pharmacist in ensuring and organising the efficient supply of medication during the patients stay in hospital and on discharge from the hospital including assessing suitability of medication for discharge.o To be proactive in the discharge planning process and liaise with the ward pharmacist and other healthcare professionals to ensure prescriptions are processed and delivered to the patients in a timely manner.o To counsel patients and their carers to ensure greater understanding of their medication including its safe use and side effects.
To undertake all clinical duties in accordance with standard operating procedure and all local, Trust and national guidelines. Ensure good team working and communication between pharmacy staff, ward pharmacist, ward staff and medical staff on behalf of the patients. To deal with queries from patients and all healthcare professionals in a friendly and courteous manner. To assist in maintaining optimal stock levels of medication on all ward areas. To participate in the training and supervision of pharmacy assistants in the ordering, maintenance, and delivery of stock for wards and departments within the Trust. To assist in the training, induction and supervision of staff involved in ward-based technician services including pre-registration trainee pharmacy technicians, pharmacy technicians, pharmacy assistants, pre-registration pharmacists and new members of staff. To complete yearly Personal Development Reviews for staff including pre-registration trainee pharmacy technicians, pharmacy technicians and pharmacy assistants. To provide pharmacy technician cover at Christie @ sites as required. To contribute to the regular review and development of the clinical service. To demonstrate awareness and commitment to the Trusts Clinical & Research Governance agenda and to implement agreed clinical & research governance initiatives. To participate in departmental, Trust and National risk management schemes such as error reporting systems and intervention monitoring. To assist in clinical audit or practice research as required. To provide annual leave/absence cover for other clinical pharmacy technicians in their duties. To undertake general dispensary duties in accordance with standard operating procedures in line with the clinical needs of ward patients. To participate in the development of the satellite pharmacy service on Oak Road Treatment Centre. To support the satellite dispensary when required and facilitate the medication requirements for chemotherapy patients. To provide dispensing and accuracy checking duties within the satellite pharmacy. To coordinate medication requirements for haematology and ambulatory care day case units. To support the monitoring and replenishment of the resuscitation boxes within the Trust. To support the cyclical medication and homecare services when required. To support the Christie at Home service when required. To participate in controlled drug destruction in line with relevant SOPs and national guidance. To contribute to any investigation at ward level regarding anomalies or discrepancies with controlled drug stock or patients own controlled drugs, stored on the ward/department or any other medication related incidents as appropriate. To liaise with the Chief Clinical Pharmacy Technician when further investigation is required regarding controlled drug incidents or any other medication related incidents if the initial investigation is not resolved. To be an accredited accuracy checking technician and to support the satellite dispensary as required. To be fully aware of the COSHH regulations particularly regarding the safe storage and handling of pharmaceutical products. To participate in Continuing Professional Development ensuring relevant knowledge and skills are up to date, meeting the professional requirements of the General Pharmaceutical Council. To participate in mandatory training in line with Trust and departmental requirements. To participate in all department rotas including the extended opening hours of the department rota, weekend service (Saturdays and Sundays) and Bank Holiday working as requested. To always behave in a manner that is in accordance with the professional standards set by the General Pharmaceutical Council. Undertake all other related duties which may be required in accordance with the changing needs and practices of the department and organisation.
Person Specification
Qualifications
Essential
- BTEC Level 3 Diploma in Pharmaceutical Science /NVQ Level 3 in Pharmacy Services or equivalent recognised pharmacy technician qualification
- BTEC Level 4 Professional Diploma in Dispensing Accuracy Checking or equivalent recognised accuracy checking qualification - or be willing to work towards the qualification
- Registration with the General Pharmaceutical Council
Desirable
- BTEC Level 4 Professional Diploma in Clinical Pharmacy Services or equivalent
- Management qualification
- Member of APTUK
- Member of BOPA
Experience
Essential
- Previous post qualification experience e.g. community or hospital experience
Desirable
- Experience of working in ward pharmacy and clinical services
- Experience within the oncology setting
- Experience of working within hospital pharmacy
Skills
Essential
- Excellent written communication skills
- Excellent verbal communication skills
- Ability to work on own initiative and as part of a team
- Good organisation and time management skills
- Ability to work under pressure, highly organised, work to deadlines
- IT literate
- Understanding of job role and responsibilities
Desirable
- Ability to influence and negotiate with medical, nursing and pharmacy staff
- Experience in supervision of other staff
Knowledge
Essential
- Good working knowledge of medicine optimisation
- Good knowledge of clinical use of medicines
Desirable
- Experience of drug use in oncology setting
Values
Essential
- Able to deal with varied situations with tact and diplomacy
- To show empathy and understanding staff and patients
- To treat people with dignity and respect
- Ability to adapt to change and to develop services and system to meet changing need
Other
Essential
- Ability to work in a busy environment and deal with several on-going commitments and tasks at the same time
- Able to contribute constructively to a team-working environment
- Able to follow general processes and procedures and working using own initiative without direct supervision
Person Specification
Qualifications
Essential
- BTEC Level 3 Diploma in Pharmaceutical Science /NVQ Level 3 in Pharmacy Services or equivalent recognised pharmacy technician qualification
- BTEC Level 4 Professional Diploma in Dispensing Accuracy Checking or equivalent recognised accuracy checking qualification - or be willing to work towards the qualification
- Registration with the General Pharmaceutical Council
Desirable
- BTEC Level 4 Professional Diploma in Clinical Pharmacy Services or equivalent
- Management qualification
- Member of APTUK
- Member of BOPA
Experience
Essential
- Previous post qualification experience e.g. community or hospital experience
Desirable
- Experience of working in ward pharmacy and clinical services
- Experience within the oncology setting
- Experience of working within hospital pharmacy
Skills
Essential
- Excellent written communication skills
- Excellent verbal communication skills
- Ability to work on own initiative and as part of a team
- Good organisation and time management skills
- Ability to work under pressure, highly organised, work to deadlines
- IT literate
- Understanding of job role and responsibilities
Desirable
- Ability to influence and negotiate with medical, nursing and pharmacy staff
- Experience in supervision of other staff
Knowledge
Essential
- Good working knowledge of medicine optimisation
- Good knowledge of clinical use of medicines
Desirable
- Experience of drug use in oncology setting
Values
Essential
- Able to deal with varied situations with tact and diplomacy
- To show empathy and understanding staff and patients
- To treat people with dignity and respect
- Ability to adapt to change and to develop services and system to meet changing need
Other
Essential
- Ability to work in a busy environment and deal with several on-going commitments and tasks at the same time
- Able to contribute constructively to a team-working environment
- Able to follow general processes and procedures and working using own initiative without direct supervision
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details
Employer name
The Christie NHS FT
Address
Pharmacy Clinical - E00920
Manchester
M20 4BX
United Kingdom
Employer's website
Employer details
Employer name
The Christie NHS FT
Address
Pharmacy Clinical - E00920
Manchester
M20 4BX
United Kingdom
Employer's website
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