Description
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.
Responsibilities:
- 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!