📍 Location: Poznań, Poland
We are looking for an experienced CRA to join our sponsor-dedicated team in Poznań. This role offers the opportunity to work exclusively with one global sponsor, providing strong study continuity, deep therapeutic exposure, and long-term career development.
🔬 Key Responsibilities:
• Conduct site monitoring visits (initiation, routine, and close-out)
• Ensure compliance with protocols, SOPs, and applicable regulations
• Perform source data verification and maintain high data quality standards
• Track and follow up on SAEs, ensuring patient safety oversight
• Prepare accurate monitoring and trip reports
• Support feasibility activities, site selection, and investigator engagement
• Collaborate closely with sponsors, investigators, and internal teams
• Contribute to training and mentoring of junior team members
🎯 Requirements:
• ~1.5 years of independent monitoring experience in Pharma/CRO
• Experience in interventional clinical studies
• Strong knowledge of SAE reporting
• Degree in Life Sciences, Nursing, or related field
• Fluency in English and Polish
• Oncology experience is a plus (or willingness to work in oncology studies)
✨ What we offer:
• Dedicated role with one global sponsor
• Exposure to complex, international clinical trials
• Clear career progression opportunities
• Supportive and collaborative team environment
Learn more about our EEO & Accommodations request here
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.
Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.
Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.
Together, exceptional is possible.
Learn more at Fortrea.com
