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)
