An excellent opportunity has arisen at the Sutton site of the Royal Marsden Hospital to work within the Department of Haemato-Oncology Unit as a Clinical Trial Coordinator on a large and varied portfolio.
Ideally with previous clinical research experience and preferably educated to degree level or equivalent, you will work within the guidelines and policies for the conduct of clinical trials, ensuring high standards of practice in accordance with the principles of GCP.
The successful applicant should have a flexible approach to their duties and the ability to work both as part of a team and independently. You will have excellent communication, administrative, and IT skills, and be supportive and open to new initiatives.
Due to the high volume of applications, we reserve the right to close the advert before the published closing date once sufficient applications are received. We advise early submission to prevent disappointment.
As we often have many applicants, we will only contact those shortlisted for interview. If you do not hear within 2 weeks of the closing date, please assume you have not been shortlisted.
Primary responsibilities include:
1. Coordination and oversight of allocated clinical trials in the Department.
2. Set-up and conduct of trials in accordance with regulatory, sponsor, and organisational requirements.
3. Ensure trials are conducted per Good Clinical Practice and Trust SOPs.
4. Review resource requirements and advise the department head accordingly.
5. Provide regular reports on departmental activity and highlight concerns.
The Royal Marsden NHS Foundation Trust is a world-leading cancer centre offering top cancer care and contributing globally to research. We employ over 4,500 staff across various careers and have facilities in Chelsea, Sutton, and Kingston.
We value life and strive for excellence in everything we do. We offer a stimulating environment, staff benefits, learning opportunities, and flexible working options. We seek employees who aspire to excellence, share our values, and contribute to our achievements.
For more details, see the attached Job Description and Person Specification.
Primary areas of responsibility:
Trial set-up:
* Liaise with R&D, pharmacy, finance, labs, and support departments to set up trials and assess capacity.
* Coordinate with Sponsors and R&D regarding trial contracts.
* Ensure material transfer arrangements are in place for tissue transfer or receipt.
* Manage essential trial documentation and maintain site files.
This advert closes on Friday, 29 August 2025.
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