Clinical Trial Administrator

Reposted 13 Days Ago
Be an Early Applicant
Dublin, IRL
In-Office
Junior
Biotech
The Role
The Clinical Trial Administrator will manage study activities, maintain documentation, ensure compliance, assist with meetings, support trial operations, and liaise with vendors.
Summary Generated by Built In

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.

Top Skills

Clinical Research Administration
Regulatory Compliance
Trial Master File Management
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The Company
HQ: Research Triangle Park, NC
10,811 Employees

What We Do

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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