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: Learn more...