Clinical Trial Manager

Clinical Trial Manager

Our client is currently looking to recruit a Clinical Trial Manager on an initial 6 month contract.

Clinical Trial Manager Central London – Hybrid £33 per hour inside IR35

An exciting opportunity has arisen for an experienced and dedicated Clinical Trial Manager to join a dynamic, academically-led Clinical Trials Unit. This role will support the delivery of a high-profile, multi-centre clinical trial and contribute to the advancement of evidence-based healthcare through rigorous, methodologically sound research.

About the Role As Clinical Trial Manager, you will be responsible for the end-to-end coordination of a complex clinical trial, working within a multidisciplinary team that includes clinicians, statisticians, IT professionals, and regulatory experts. The role is integral to the successful setup, conduct, and reporting of academic-led trials with a focus on quality, compliance, and patient safety. Key responsibilities include:

• Leading trial setup activities including protocol implementation, approvals, and site initiation
• Ensuring compliance with UK Clinical Trial Regulations, ICH-GCP, and institutional SOPs
• Acting as the primary liaison between the Trials Unit, participating sites, and Chief Investigator
• Coordinating trial communications, documentation, and progress reporting
• Overseeing data quality, monitoring activities, and safety reporting
• Supporting academic dissemination through presentations and reports to committees and funding bodies

About You You will have a strong background in clinical trial management and a good understanding of academic research environments. The role requires a methodical, solutions-focused approach, excellent interpersonal skills, and the ability to work independently within a supportive, collaborative team. Essential criteria:

• Degree or equivalent experience in clinical trials or a related field
• Proven experience managing interventional trials, including IMP studies
• In-depth knowledge of UK regulations, GCP, and the Research Governance Framework
• Excellent organisational skills and the ability to manage competing deadlines
• Strong communication skills and experience liaising with multiple stakeholders
• Proficiency with clinical trial management systems and Microsoft Office

Desirable:

• Previous experience working in academic or NHS research settings
• Experience in pharmacovigilance and data management
• Ability to supervise or mentor junior staff
• Commitment to equity, diversity, and inclusion in research

This role offers a unique opportunity to contribute to cutting-edge research within an established academic trials infrastructure. If you are passionate about improving healthcare through clinical research and enjoy working in a collaborative academic environment, we encourage you to apply.