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.