Clinical Trial Administrator

The role

Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London.

This client-dedicated role is to be office based in central London for at least 3 days a week with the rest of the time being spent working from home. Ideally you will have at least 1-2 years experience of supporting Clinical Trials in the UK.

Much of the work will involve complex oncological clinical trials, providing valuable opportunities to develop your skills and expertise.

• Communicate with project teams and track study activities
• Maintain essential documentation and regulatory compliance
• Support site and study material preparation
• Assist with meeting coordination, minute-taking, and documentation
• Manage Trial Master File (TMF) documentation and quality control
• Liaise with vendors and coordinate study supply shipments
• Provide general administrative and systems support

• A minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company - this is essential!
• Must be within commuting distance of Central London (office-based 3 days per week)
• Basic understanding of biology and biological processes
• Good organizational and time management skills

This role is a full time & permanent position to be employed through Fortrea.

This is a great opportunity to gain hands-on experience in clinical research and contribute to high-quality clinical data production.

Learn more about our EEO & Accommodations request here.