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. This role is a full time & permanent position to be employed through Fortrea.
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
If you thrive in a fast-paced environment and enjoy working with a dynamic team,
At Fortrea, we’re all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence.
Regardless of your role, we’re all family, working together to achieve extraordinary results.
At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.
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Contact Details:
FTMAI Fortrea Development Ltd Recruitment Team
