Fortrea is currently seeking a proactive In-house Clinical Research Associate to join our expanding team in the UK. This is a home-based role.

REQUIREMENTS:

• Minimum of 12 months’ experience in Clinical Research Administration (e.g. Study Coordinator, CRA internship etc)
• Experience supporting clinical trials in the UK is preferred
• Strong ability to work independently and manage time effectively
• Basic understanding of biology and clinical trial processes
• Excellent organizational and communication skills

✅ Communicate with project teams and track study activities
✅ Maintain essential documentation and ensure 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