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Clinical Trials Coordinator - Research & Development

East and North Hertfordshire NHS Trust

Medical Protection — indemnity for locally employed doctors from £79
Location
Stevenage, England
Salary
£28,392 - £31,157 per annum plus 15% High Cost Area Supplement
Profession
Administrative and IT
Grade
Band 4
Deadline
03 Jun 2026
Contract Type
Fixed term: 12 months (End Date: 12 Months from Start Date)
Posted Date
21 May 2026

Job overview

We are recruiting for a Clinical Trials Coordinator who shares our vision to be trusted to provide consistently outstanding care and exemplary service to our patients.

An exciting opportunity has arisen to join our Research team based at Mount Vernon Cancer Centre in Northwood, London for a 12-month period. The post involves working alongside Research Nurses and Clinicians to deliver research trials.

The main purpose of the role is to support the clinical research 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 Research Nurses and wider Clinical Research Team.

You will be joining a well-established Research Team and a department which has over 100 members of research staff throughout the Trust.

In addition, you will receive a High-Cost Area Supplement of 15% of your basic salary, subject to a minimum payment of £4,870 and a maximum payment of £6,137 per annum pro rata.

At the heart of everything we do are our core values: Include, Respect, and Improve. We encourage you to embrace these values throughout the recruitment process and in your role with us.

Main duties of the job

The Clinical Trials Coordinator will assist with the efficient and timely set up of clinical trials.

Maintain databases/spreadsheets and produce monthly progress reports on recruitment.

Assist with the tracking and raising of invoices. Identifying discrepancies and escalating appropriately.

Manage own workload for daily trial activity including case report form completion and amendment processing to meet internal and external deadlines.

Assist with quality assurance of all trial related documentation in accordance with relevant legislation and guidelines.

Assist with preparation for audit and inspections within assigned teams.

General trial-related communication in accordance with the Data Protection Act.

Detailed job description and main responsibilities

Please see the attached Job Description and Person Specification applicant pack for further detailed information regarding this role.

ENHT is seeking to maintain and expand the Mount Vernon Cancer Centre staff as we move to an exciting new future.

We welcome applications from those who would relish the opportunity to be part of new and developing cancer service, building on the excellent reputation, research and patient experience the Cancer Centre already delivers.