Clinical Trial Manager
London
Posted 19 days ago
Contract
Clinical Trial Manager (CTM) – 6-Month Contract
A global leader in rare genetic disease therapeutics is seeking an experienced Clinical Trial Manager (CTM) to join their Global Study Operations team on a 6-month contract. This role is responsible for the end-to-end management and delivery of clinical studies, ensuring timelines, quality, and budget targets are consistently met.
About the Role: As a Clinical Trial Manager (CTM), you will take ownership of clinical study execution across Phase 1 through post-approval. You will lead cross-functional teams, oversee vendors, and ensure studies are delivered on time, within budget, and in compliance with regulatory requirements. This is a highly visible role with direct impact on advancing innovative therapies for rare diseases.
What You’ll Do: Lead global clinical trial execution from study start-up through close-out Oversee CROs and external vendors to ensure performance, quality, and delivery Drive study timelines, budgets, and risk management strategies Ensure compliance with GCP, regulatory requirements, and internal SOPs Lead study team meetings and act as the primary point of contact for study operations Oversee site management, monitoring strategy, and issue resolution Review and approve key study documents (protocols, plans, reports) Ensure accurate and timely maintenance of Trial Master Files (TMF) Partner cross-functionally with Clinical, Regulatory, Data Management, and Safety teams Provide operational leadership and escalation management as needed
Who You Are: A confident study leader with strong project management capabilities Proactive, solutions-oriented, and able to manage complexity Experienced in global clinical trial delivery and vendor oversight Strong communicator with the ability to influence cross-functional stakeholders Detail-oriented while maintaining a strategic, big-picture perspective
Qualifications: BSc or higher in nursing, life sciences, or related field (or equivalent experience) Significant experience in clinical trial management within pharma/biotech Proven experience managing CROs and external vendors Strong knowledge of drug development processes and regulatory requirements (GCP, ICH) Experience across multiple study phases preferred
Ready to help transform rare disease care? Apply now to play a key role in delivering life-changing therapies to patients worldwide.
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