NHS Logo

Clinical Trial Coordinator

The Royal Marsden NHS Foundation Trust
This job is closed to applications
Medical Protection Advertisement

Location
Salary
£34,521 - £41,956 per annum
Profession
Administrative and IT
Grade
Band 5
Deadline
28 Jul 2025
Contract Type
11 months (Fixed term: 11.5 months)
Posted Date
14 Jul 2025

Job overview

linical Trial Coordinator, Lung and Mesothelioma Research.  The Royal Marsden NHS Foundation Trust has an international reputation for high quality patient care, education and research and its partnership with The Institute of Cancer Research (ICR) has created the largest comprehensive cancer centre in Europe.

This role is based within the Lung Research Team at The Royal Marsden (located at two sites – Sutton, Surrey and Chelsea, London), which is world renowned for excellence in clinical care and clinical research. Applications are invited for a Clinical Trial Coordinator role which is a 12 month fixed-term post, with possibility of extension.

For further details contact: [email protected]

Main duties of the job

  • Responsible for the day-to-day coordination and oversight of allocated clinical trials in the Department.
  • Responsible for the set-up and conduct of allocated clinical trials in accordance with regulatory, sponsor and organisational requirements.
  • Ensure clinical trials within the Unit are conducted in accordance with Good Clinical Practice and Trust SOPs.
  • Review the capacity and resource requirements within the Clinical unit for coordination and administrative management of the allocated trials and to advise the unit head accordingly.
  • To be an active member of the department, providing regular reports on activity within the Department and highlighting areas of concern.

Detailed job description and main responsibilities

For further information on this role, please see the attached detailed Job Description and Person Specification:

  • To be responsible for maintaining own professional development and be aware of current practices and future developments within the Trust and National Health Service.
  • To aid in the implementation of corrective and preventative measures within the Unit as agreed with the Unit Head.
  • To support the Clinical R&D Office in preparation for regulatory inspections.
  • To take an active role in the Unit and the Trust as a member of a clinical research team.
  • To help coordinate the Unit’s research meeting ensuring appropriate, documented monitoring of the clinical trial portfolio.