Fortrea is currently seeking a proactive Clinical Trial Administrator to join our expanding team in Ireland. This is a home-based role, but occasional travel to our Dublin office will be required. You will be working exclusively on Irish studies, so the ability to work independently and take ownership of your tasks is essential.
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.
