Overview
An exciting opportunity has arisen to join The Royal Marsden Clinical Trials Unit as a Trial Manager in the RM-CTU Breast team. This is an ideal position for a data manager looking to progress in their career or a trial manager/co‑ordinator wishing to learn more about oncology drug trials from the sponsor perspective. You will join a team of experienced trial professionals, world‑class clinicians and scientists based in the Ralph Lauren Centre for Breast Cancer Research and be part of groundbreaking research into breast cancer treatments.
Flexible working hours and hybrid working in office/at home are supported in this team.
Responsibilities
* Take responsibility for at least one clinical trial, including maintenance of the Trial Master File, key study documentation and obtaining relevant ethical and regulatory approvals.
* Safety reporting of adverse events, monitoring trial progress and facilitating meetings.
* Produce reports for various stakeholders.
* Coordinate all activities required for the effective running of clinical trials and other studies in the portfolio.
* Undertake project management for the studies, working with other departments within the Royal Marsden Hospital as well as sites, funders, external collaborators and contractors.
* Support and actively engage in the creation of the documentation required for each study, including amendments and submissions to regulatory authorities.
* Lead the team by supervising and supporting junior staff.
* Contribute to the RM‑CTU development and strategy, including review of SOPs, policies and processes.
* Lead the implementation of systems within the Unit to ensure clinical trials are conducted in accordance with all regulatory internal requirements.
* Be the main point of contact for the clinical R&D office for the set‑up and management of an assigned portfolio of clinical trials.
* Assist in preparation for audits and regulatory inspections.
Service Delivery
* Ensure high standards of practice in accordance with the principles of GCP.
* Excellent communication and organisational skills.
* Ability to work proactively and independently.
* Good time‑management skills and ability to prioritise competing workloads.
Qualifications
* Prior relevant experience of working on clinical trials, either from within the NHS, industry or academic sector.
For further information and informal queries please contact: Dymphna Lee, Lead Project Manager – RM‑CTU Breast team, Dymphna.lee@rmh.nhs.uk.
This advert closes on Monday 27 Oct 2025.
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