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 .