Clinical trial coordination and regulatory expertise are central to this full time Sutton position with The Royal Marsden NHS Foundation Trust.

As a Senior Clinical Trial Coordinator, you will support commercial and non-commercial CTIMP portfolios within the GI and Lymphoma Unit. The work covers regulatory submissions, costing, trial setup, daily coordination, closeout, and archiving. You will help deliver protocols under Good Clinical Practice, Data Protection, Research Governance, and Trust Standard Operating Procedures.

Key Responsibilities:

- Manage hosted studies within the clinical unit
- Coordinate assigned trials through setup and closeout
- Ensure protocols meet statutory and regulatory requirements
- Convey Clinical R&D; Office requirements to clinical staff




- Represent the unit at key meetings when required

Requirements:

- At least three years coordinating CTIMP research and trials
- First degree in life science or health-related subject
- Three years’ experience with Good Clinical Practice
- Understanding of Data Protection and Research Governance
- Experience in a clinical trials unit, CRO, or pharmaceutical company

Bring experienced clinical trial coordination, regulatory knowledge, and organised delivery to The Royal Marsden’s Sutton research unit.

📌 Senior Clinical Trial Coordinator (Sutton)
🏢 The Royal Marsden NHS Foundation Trust
📍 Sutton