Fortrea is currently seeking a proactive Clinical Trial Administrator to join our expanding team. This is a home-based role, but you must be based in Ireland with full right to work in Ireland. To be considered, you should have at least one year of prior Clinical Trial Administrator experience. While primarily remote, occasional travel to our Dublin office may be required.

What You’ll Do:

✅ Communicate with project teams and track study activities for Irish trials
✅ 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

Requirements:

Minimum of 12 months’ experience in Clinical Research Administration (CRO or Pharma)
Experience supporting clinical trials in Ireland is preferred
Strong ability to work independently and manage time effectively
Basic understanding of biology and clinical trial processes
Excellent organizational and communication skills

Why Join Us?

This role offers the flexibility of home-based work while giving you the opportunity to be part of complex, high-quality clinical trials in Ireland. You’ll have a chance to develop your skills in a supportive and growing team, working on impactful studies.

Learn more about our EEO & Accommodations request here.

Clinical Trial Administrator

Job Description