Clinical Trial Administrator London

**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. **What You’ll Do:** ✅ 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 **Requirements:** * 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. If you thrive in a fast-paced environment and enjoy working with a dynamic team, we’d love to hear from you! Learn more about our [EEO & Accommodations request here](https://careers.fortrea.com/us/en/eeo-and-accommodations).