About the role
Fortrea is looking for a CRA I to join our multisponsor team in Central Poland , with a preference for candidates based in or near Warsaw . This is an exciting opportunity to gain exposure to a variety of clinical studies while growing your monitoring career within a global CRO.
What you'll do
- Perform on-site and remote monitoring visits in line with study protocols, ICH-GCP, and regulatory requirements.
- Support sites from study start-up through close-out.
- Review source data and ensure data quality and patient safety.
- Build strong relationships with investigators and site staff.
- Track study progress and prepare monitoring reports.
- Support audit and inspection readiness.
What we're looking for
- Life science degree, nursing qualification, or equivalent scientific background.
- At least 6 months to 1 year of independent site monitoring experience as a CRA.
- Experience in interventional clinical trials.
- Good understanding of ICH-GCP and clinical trial processes.
- Strong communication, organizational, and problem-solving skills.
- Fluent in Polish and English .
- Willingness to travel within Poland.
Why Fortrea?
- Join a supportive and collaborative team.
- Work across a variety of therapeutic areas and studies.
- Gain valuable experience in a multisponsor environment.
- Access clear career development opportunities and ongoing training. Be part of a global organization helping bring innovative treatments to patients.
Interested? Apply today and continue building your CRA career with Fortrea.
Learn more about our EEO & Accommodations request here .
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