Senior Clinical Trial Management Associate
SCTMA_4311860757
Posted: 09/10/2025
- London Area, United Kingdom (Hybrid)
- Contract
Job Title: Senior Clinical Trials Management Associate
Location: Hybrid (3 days onsite per week) – London
Contract Type: 12-month Contract
Therapeutic Area: Oncology / Cell Therapy
About the Role:
An exciting opportunity has arisen for a Senior Clinical Trials Management Associate to join a leading biopharmaceutical company specialising in innovative cancer immunotherapies. As part of the Clinical Operations team, you will support the execution of global Phase 1–4 clinical trials with a strong focus on oncology and advanced cell therapies.
This role is offered on a hybrid basis, with 3 days onsite in London and the remainder remote.
Key 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).
About You:
You are a detail-oriented clinical research professional with strong organisational skills and a passion for improving outcomes in oncology. You thrive in a collaborative environment and are confident working across global teams.
Requirements:
- Degree in a life science or related discipline (or equivalent experience).
- Solid experience in clinical trials, ideally within pharma, CROs, or clinical sites.
- CRA background is highly desirable.
- Oncology experience is essential; CAR-T Cell Therapy experience is a strong plus.
- Strong understanding of ICH GCP and regulatory guidelines (FDA/EMA).
- Skilled in MS Word, PowerPoint, and Excel.
- Excellent verbal, written, and interpersonal communication skills.
- Knowledge of European clinical trial regulations is advantageous.
Interested?
If you're ready to join a fast-paced, purpose-driven environment and contribute to life-changing oncology research, we’d love to hear from you.
Sashmika Sakthi
Senior Candidate Consultant
