Clinical Trial Manager

  • 4M Recruitment
  • Jul 23, 2025
Contractor Healthcare & Medical Management

Job Description

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.