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Clinical Trial Administrator, London, Maidenhead
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Client:
Location:
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
7953aeb0b418
Job Views:
5
Posted:
05.05.2025
Expiry Date:
19.06.2025
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Job Description:
The role
Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London.
This client-dedicated role is 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 of supporting Clinical Trials in the UK.
Much of the work involves 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. #J-18808-Ljbffr