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Clinical Research Nurse / Practitioner
Queen Victoria Hospital NHS Foundation Trust View all jobs
Posted 19 day(s) ago
Reference: 276-8285372-AC
Job summary
We are looking for an experienced Research Nurse / Research Practitioner (CRP) - Part-time (24 hours per week)to join the Research and Innovation team at Queen Victoria Hospital.
We undertake work across a range of specialties, which means plenty of variety in the role - from questionnaire studies right up to full scale clinical drug/device trials. You'll need good organisational skills, high attention to detail, and considerable experience working in clinical research.
This is an excellent opportunity for a motivated research nurse or practitioner who can work independently while contributing actively to a supportive multidisciplinary research team.
Main duties of the job
The postholder will coordinate a portfolio of clinical research studies across the Trust's specialist services. They will identify and recruit eligible participants, support informed consent, coordinate research-related assessments and follow-up, and maintain accurate study documentation and data.
Working closely with principal investigators, clinical teams, support departments, sponsors and research networks, the postholder will help ensure that studies are set up and delivered safely, efficiently and in accordance with the protocol, Good Clinical Practice and applicable research governance requirements.
About us
Rated GOOD overall with outstanding care by the CQC. A specialist NHS hospital providing life-changing reconstructive surgery, burns care and rehabilitation services across the South of England and beyond.
We specialise in conditions of the eyes (corneoplastics), hands, head and neck cancer and skin cancer, reconstructive breast surgery, maxillofacial surgery and prosthetics, providing regional and national services in these areas of clinical expertise.Our world-leading clinical teams also treat more common conditions of the eyes, hands, skin, and teeth for the people of East Grinstead and the surrounding areas. In addition, QVH provides a minor injuries unit, expert therapies, a sleep service, and a growing portfolio of community-based services.Patients consistently rate QVH amongst the top hospitals in the country for quality of care.
Our success is underpinned by the skills and enthusiasm of our staff and a strong culture of partnership. We are fully committed to training and development of the workforce with support for continuing education and learning.
Details
Date posted
14 September 2026
Pay scheme
Agenda for change
Band
Band 6
Salary
£39,959 to £48,117 a year per annum
Contract
Permanent
Working pattern
Part-time
Reference number
276-8285372-AC
Job locations
Queen Victoria Hospital
Holtye Road
East Grinstead
RH19 3DZ
United Kingdom
Job description
Job responsibilities
The postholder will:
- Coordinate the research-related care of participants enrolled in a designated portfolio of studies.
- Identify potentially eligible participants through clinics, operating lists, clinical referrals.
- Provide clear study information to patients, families and carers and undertake informed consent where trained, delegated and competent to do so.
- Coordinate protocol-required assessments, investigations, sample collection, treatment and follow-up.
- Collect, process, store and dispatch biological samples according to study protocols.
- Monitor participants for adverse events and ensure that safety information is documented, escalated and reported within required timelines.
- Maintain accurate source documentation, case report forms, electronic study systems and local research databases.
- Maintain inspection-ready study documentation and support monitoring visits, audits and inspections.
- Lead study feasibility, set-up and initiation, including liaison with principal investigators, sponsors and supporting departments.
- Monitor recruitment performance, identify barriers and contribute to actions that improve patient access and study delivery.
- Promote research awareness among clinical teams.
- Deliver studies to a consistently high standard in accordance with the approved protocol, ICH Good Clinical Practice, applicable UK Clinical Trials Regulations, the UK Policy Framework
Job description
Job responsibilities
The postholder will:
- Coordinate the research-related care of participants enrolled in a designated portfolio of studies.
- Identify potentially eligible participants through clinics, operating lists, clinical referrals.
- Provide clear study information to patients, families and carers and undertake informed consent where trained, delegated and competent to do so.
- Coordinate protocol-required assessments, investigations, sample collection, treatment and follow-up.
- Collect, process, store and dispatch biological samples according to study protocols.
- Monitor participants for adverse events and ensure that safety information is documented, escalated and reported within required timelines.
- Maintain accurate source documentation, case report forms, electronic study systems and local research databases.
- Maintain inspection-ready study documentation and support monitoring visits, audits and inspections.
- Lead study feasibility, set-up and initiation, including liaison with principal investigators, sponsors and supporting departments.
- Monitor recruitment performance, identify barriers and contribute to actions that improve patient access and study delivery.
- Promote research awareness among clinical teams.
- Deliver studies to a consistently high standard in accordance with the approved protocol, ICH Good Clinical Practice, applicable UK Clinical Trials Regulations, the UK Policy Framework
Person Specification
Skills
Desirable
- Competency in phlebotomy, ECG and other relevant clinical activities
Qualifications
Essential
- NMC registration, relevant professional registration (eg. CRP accreditation) or equivalent experience
- Evidence of continuing professional development
Experience
Essential
- Experience of delivering research studies including CTIMPs and device trials
- Experience in new study feasibility and set-up
- Experience of dealing with patients and families in distress
- Experience of working with different study databases and clinical research management system (eg. EDGE)
- Experience of using MS office package (Excel, PowerPoint, Word)
Desirable
- Experience of the care of cancer patients
- Experience in ophthalmic care
- Experience in plastic surgery specialty
Knowledge
Essential
- Knowledge of the clinical research life-cycle; from EOI, feasibility, and set-up to coordination and closure--including securing all regulatory approvals prior to recruitment initiation
Qualifications
Essential
- Knowledge of ICH-GCP, Clinical Trial Regulation 2004 and UK Policy Framework
Skills
Essential
- Organisation, problem solving and management skills
- Interpersonal skills and able to communicate complex information at all level
- Ability to analyse complicated information from trial protocol
- Sound prioritising skills and ability to manage own workload
Person Specification
Skills
Desirable
- Competency in phlebotomy, ECG and other relevant clinical activities
Qualifications
Essential
- NMC registration, relevant professional registration (eg. CRP accreditation) or equivalent experience
- Evidence of continuing professional development
Experience
Essential
- Experience of delivering research studies including CTIMPs and device trials
- Experience in new study feasibility and set-up
- Experience of dealing with patients and families in distress
- Experience of working with different study databases and clinical research management system (eg. EDGE)
- Experience of using MS office package (Excel, PowerPoint, Word)
Desirable
- Experience of the care of cancer patients
- Experience in ophthalmic care
- Experience in plastic surgery specialty
Knowledge
Essential
- Knowledge of the clinical research life-cycle; from EOI, feasibility, and set-up to coordination and closure--including securing all regulatory approvals prior to recruitment initiation
Qualifications
Essential
- Knowledge of ICH-GCP, Clinical Trial Regulation 2004 and UK Policy Framework
Skills
Essential
- Organisation, problem solving and management skills
- Interpersonal skills and able to communicate complex information at all level
- Ability to analyse complicated information from trial protocol
- Sound prioritising skills and ability 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
Queen Victoria Hospital NHS Foundation Trust
Address
Queen Victoria Hospital
Holtye Road
East Grinstead
RH19 3DZ
United Kingdom
Employer's website
https://www.qvh.nhs.uk/ (Opens in a new tab)
Employer details
Employer name
Queen Victoria Hospital NHS Foundation Trust
Address
Queen Victoria Hospital
Holtye Road
East Grinstead
RH19 3DZ
United Kingdom
Employer's website
https://www.qvh.nhs.uk/ (Opens in a new tab)