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.