About this 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.