Lead clinical trial management for The Royal Marsden’s Gastro-intestinal and Lymphoma Unit, applying regulatory expertise at the London site as needed. This full time role covers maternity leave for 14 months.
As Senior Trial Manager, you will coordinate studies from protocol development through reporting and archiving. The work requires clinical trial project management, IRAS submissions, costings, and Good Clinical Practice knowledge. You will support research into gastro-intestinal cancer and lymphoma.
Key Responsibilities: Coordinate activities required for effective clinical trial delivery
Manage studies with departments, sites, funders, collaborators, and contractors
Create study documentation, amendments, submissions, and regulatory reports
Lead and supervise junior team members




Develop systems for efficient multicentre study management
Requirements: Experience setting up and managing clinical trials
Clinical trial project management experience from protocol to archiving
Experience preparing IRAS submissions for MHRA and ethics committees
First degree in life science or health-related subject
Working knowledge of GCP, Data Protection, and Research Governance
Use clinical trial leadership, regulatory submissions, and project management expertise to support oncology research at The Royal Marsden.

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📌 Senior Clinical Trial Manager (Saskatchewan)
🏢 The Royal Marsden NHS Foundation Trust
📍 Saskatchewan