# Clinical Research Nurse/Clinical Research Practitioner

> NHS job listing from Job Clerk for East Sussex Healthcare NHS Trust.

## Canonical URLs

- **HTML:** https://www.jobclerk.com/job/clinical-research-nurseclinical-research-practitioner/8d24a933-9ddc-4604-b068-33898991153f
- **Markdown:** https://www.jobclerk.com/job/clinical-research-nurseclinical-research-practitioner/8d24a933-9ddc-4604-b068-33898991153f.md

## Summary

- **Status:** Live
- **Employer:** East Sussex Healthcare NHS Trust
- **Location:** Eastbourne District General Hospital
- **Workplace type:** onsite
- **Profession:** Nurse (adult and children)
- **Grade:** Band 6
- **Salary:** £39,959 - £48,117 Pro rata, per anum
- **Contract type:** Fixed term: 12 months (up to)
- **Employment type:** Part time - 26 hours per week (Mon - Fri,  8am-4pm)
- **Closing date:** 2026-09-22T22:59:00.000Z
- **Posted:** 2026-09-08T08:50:43.899Z
- **Source information URL:** https://www.healthjobsuk.com/job/UK/East_Sussex/Eastbourne/East_Sussex_Healthcare_NHS_Trust/Oncology/Oncology-v8279360
- **Application URL:** https://apps.trac.jobs/job-advert/8279360?ShowJobAdvert=&feedid=9002
- **Employer website:** https://www.esht.nhs.uk

## Job Content

### Job overview

We are looking for an enthusiastic Clinical Research Nurse or Clinical Research Practitioner to join the Research & Development team at East Sussex Healthcare NHS Trust. In this key Band 6 role, you will support the delivery of an expanding portfolio of commercial and academic clinical trials, helping the Trust advance high‑quality, evidence‑based patient care.

You will independently manage a caseload of trial participants and work closely with multidisciplinary teams across our research sites. Key responsibilities include identifying, recruiting, educating and monitoring patients involved in clinical studies, ensuring all activity complies with ICH‑GCP, the UK Policy Framework for Health & Social Care Research, and local governance requirements.

Using your clinical expertise and understanding of study protocols, you will deliver research interventions, complete trial‑specific assessments, collect accurate data and maintain compliant study documentation. You will also support study feasibility, set‑up, regulatory submissions and capacity & capability processes.

The ideal candidate will be an experienced clinician or research practitioner with excellent communication and organisational skills, confidence working autonomously, and the ability to collaborate with clinical teams, research networks, sponsors and trial units. You will act as a knowledgeable resource for patients and colleagues and contribute to supervising junior research staff while upholding the Trust’s values.

### Main duties of the job

Key Responsibilities

- Support the set‑up, coordination and governance processes for clinical trials.
- Identify, recruit and consent eligible participants, ensuring clear communication and informed decision‑making.
- Deliver trial‑specific clinical procedures and monitor patients throughout their research pathway.
- Maintain accurate study documentation, data entry and record management in line with GCP standards.
- Work collaboratively with multidisciplinary teams, research sponsors and support services.
- Manage a personal caseload independently while supporting junior research staff.
- Ensure compliance with research policies, safety standards and recruitment targets.

### Detailed job description and main responsibilities

Please see attached the job description

If you have any questions please feel free to get in touch.

### Applicant requirements

You must have appropriate UK professional registration.

This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.

## Person Specification

### Experience

**Essential**

- Adequate level of post registration experience (nurse only).
- Current level of competency in a clinical specialty or, Research
- Knowledge of requirements of Good Clinical Practice and Research Governance

**Desirable**

- Proven understanding of clinical governance and risk management, its importance and application.
- Evidence of continuing professional development

### Qualifications

**Essential**

- RN / RSCN / RN(child) / RODP (Nurse Only) RN / RSCN / RN(child) / RODP (Nurse Only)
- Graduate level qualification (or equivalent experience)
- Clinical Trial Research experience (minimum12 months experience)

**Desirable**

- Good Clinical Practice qualification
- Clinical Trial Practitioner Registration (or working towards)

## Documents

- [jhf (pdf, 872.3kb)](https://www.healthjobsuk.com/documents?vdoc=10595688)
- [b6 haem_onc rn jd (pdf, 224.6kb)](https://www.healthjobsuk.com/documents?vdoc=10595686)
- [b6 rn_pract. hazard form (pdf, 503.9kb)](https://www.healthjobsuk.com/documents?vdoc=10595687)
- [guidance for applicants - afc (pdf, 152.4kb)](https://www.healthjobsuk.com/documents?edoc=672)

## Agent Notes

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