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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