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
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Perform on-site and remote monitoring visits in line with study protocols, ICH-GCP, and regulatory requirements.
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Support sites from study start-up through close-out.
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Review source data and ensure data quality and patient safety.
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Build strong relationships with investigators and site staff.
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Track study progress and prepare monitoring reports.
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Support audit and inspection readiness.
What we’re looking for
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Life science degree, nursing qualification, or equivalent scientific background.
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At least 6 months to 1 year of independent site monitoring experience as a CRA.
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Experience in interventional clinical trials.
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Good understanding of ICH-GCP and clinical trial processes.
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Strong communication, organizational, and problem-solving skills.
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Fluent in Polish and English.
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Willingness to travel within Poland.
Why Fortrea?
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Join a supportive and collaborative team.
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Work across a variety of therapeutic areas and studies.
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Gain valuable experience in a multisponsor environment.
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Access clear career development opportunities and ongoing training.
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Be part of a global organization helping bring innovative treatments to patients.
Interested? Apply today and continue building your CRA career with Fortrea.
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