Fortrea is currently seeking a proactive In-house Clinical Research Associate to join our expanding team in Poland. This is a hybrid role with 3 days working from our Warsaw office and the rest of the week remote.
What You’ll Do:
✅ Communicate with project teams and track study activities for Polish 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 (e.g. Study Coordinator, CRA internship etc)
- Experience supporting clinical trials in Poland 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 provides an excellent opportunity to support CRAs in the delivery of complex, high-quality clinical trials in Poland. It’s a chance to develop your skills in a supportive team and contribute to impactful studies.
Learn more about our EEO & Accommodations request here.
