CRA II - Sponsor Dedicated, Poznań

Job description

📍 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 .