Senior Clinical Trial Management Associate

Senior Clinical Trial Management Associate

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 aSenior 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 ahybrid basis, with3 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 isessential; 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.

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