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AI Summary
Perform clinical site monitoring activities including initiation, routine visits, and close-outs to ensure data quality and patient safety. Manage clinical sites in accordance with project plans, SOPs, and regulatory requirements while collaborating with sponsors and investigators.
We are hiring an experienced CRA II to join our sponsor‑dedicated team in Poland. In this role, you’ll work exclusively with one sponsor, gaining deep study knowledge and long‑term project ownership, with strong opportunities for career growth.
Key Responsibilities
- Perform site monitoring activities (initiation, routine monitoring, and close‑out visits)
- Manage clinical sites in line with project plans, SOPs, and regulatory requirements
- Ensure patient safety, data quality, and audit readiness
- Review CRFs, perform source data verification, and resolve queries
- Track and follow up on Serious Adverse Events (SAEs)
- Prepare accurate monitoring and trip reports
- Support feasibility, QC visits, investigator recruitment, and regulatory submissions
- Collaborate with sponsors, investigators, and internal teams
- Support training and mentoring of new team members
Requirements
- University degree in Life Sciences or Nursing
- Minimum 2 years of independent monitoring experience in Pharma/CRO
- Experience in interventional studies
- Strong knowledge of SAE reporting
- Oncology experience is a plus (or willingness to work in Oncology)
- Fluent English and Polish
Why join?
- Dedicated to one sponsor
- Exposure to complex, international studies
- Clear career progression
- Supportive and collaborative team environment
Learn more about our EEO & Accommodations request here.
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