The roleFortrea 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 supportRequirements: 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 processesGood organizational and time management skillsThis 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 .