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 Youll 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. Youll 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.
Required Experience:
Unclear Seniority
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 ...
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 Youll 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. Youll 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.
Required Experience:
Unclear Seniority
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