Location
The Royal Marsden Chelsea

Hours
Full Time (hours not specified)

Salary
£36,943 per annum

About the Role
As a Clinical Trial Coordinator, you will initiate and manage the day-to-day running of allocated clinical trials in accordance with Good Clinical Practice (GCP) and The Royal Marsden / Institute of Cancer Research (ICR) Standard Operating Procedures (SOPs). You will be responsible for completing applications to Research Ethics Committees (REC), Medicines and Healthcare products Regulatory Agency (MHRA), and Committee for Clinical Research (CCR)/R&D for new research proposals. You will ensure that trials do not commence until all regulatory, sponsor, and local R&D requirements are satisfied. Your role includes maintaining delegation logs and training records for staff working on trials, liaising with commercial companies and funders to establish funding and sponsor contracts, and ensuring adequate drug supply throughout the trial duration. You will coordinate with R&D to ensure appropriate material transfer arrangements for trials involving tissue transfer or receipt. Additionally, you will be responsible for the compilation and maintenance of essential trial documentation in Trial Master Files, Trial Site Files, and electronic files. Collaboration with pharmacy, finance, contracts, and laboratories will be key in trial setup. You will also assist with data entry and review for commercially hosted clinical trials.

Experience
Experience in clinical trial coordination or related clinical research roles is desirable. Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements is essential.

About you
You are organized, detail-oriented, and able to manage multiple tasks efficiently. You have excellent communication skills to liaise effectively with internal teams, commercial partners, and regulatory bodies. You are proactive in ensuring compliance with all trial-related procedures and documentation standards.

Qualifications
A relevant degree or equivalent experience in clinical research or healthcare is preferred. Training or certification in Good Clinical Practice (GCP) is advantageous.