Senior Clinical Trial Management Associate - London
Only for registered members London, United Kingdom
4 weeks ago
* This salary range is an estimation made by beBee
Job summary
An exciting opportunity has arisen for a Senior Clinical Trials Management Associate to join a leading biopharmaceutical company specialising in innovative cancer immunotherapies.
Responsibilities
- Support Global Trial Managers with study start-up, including vendor and central lab set-up, and coordination with CROs for timely site initiation.
- Attend accompanied visits with CRO CRAs (PSSVs, SIVs, RMVs) to ensure protocol and SOP compliance.
- Assist with the review of clinical documents such as protocols, informed consent forms, case report forms (CRFs), monitoring plans, and study reports.
- Collaborate with cross-functional teams including Regulatory Affairs, Clinical Research, Materials & Logistics, and Drug Safety to support study execution.
- Contribute to CRO and vendor oversight to ensure high-quality deliverables.
- Assist in the organisation of international investigator meetings.
- Support the preparation of safety, interim, and final study reports; assist in resolving data queries.
- Complete administrative tasks as assigned in a timely and accurate manner.
- Occasional travel required (1–2 times per year).
Job description
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