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.