Clinical Trials Manager

Overview

As a Clinical Trial Manager, you will lead trial coordination for a multicentre randomised CTIMP evaluating hormone replacement therapy for hand osteoarthritis. You will work closely with the CI, sponsors, funders, and sites to ensure recruitment, data quality, and regulatory compliance. The role sits within the ICTU framework, delivering on protocol and ICH-GCP standards within time and budget. You’ll drive study setup, stakeholder communication, and site performance in a world‑leading institution that aims to advance science for humanity. This is an opportunity to shape a NIHR‑funded trial from setup to closeout and impact patient care.

Pay / Benefits

• sector-leading salary and remuneration package
• 43 days’ annual leave
• flexible working policy from day one
• on-site leisure facilities
• cycle-to-work scheme
• travel season ticket loan

Responsibilities

• Coordinate study set-up and governance
• Liaise with Chief Investigator, collaborators, Sponsor, Funder, and advisory bodies
• Oversee progress and performance of investigator sites
• Ensure efficient recruitment and reliable data collection
• Implement ICTU systems and processes
• Ensure compliance with protocol, SOPs, regulatory and ethical requirements, and ICH-GCP
• Deliver trial on time and within budget

Key requirements

• Bachelor’s degree or equivalent in a biomedical/scientific field
• Proven clinical trial experience in multi-centre randomised trials including CTIMPs
• Willingness to travel domestically within the UK and work flexible hours

• Strong communication and stakeholder management
• Team collaboration and cross-functional coordination
• Adaptability and problem-solving under timelines
• CTIMPs experience
• ICH-GCP compliance
• Experience with trial management systems and data collection processes

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