CRA II - FSP, Romania

This may be time for you to join our innovative FSP team as a Clinical Research Associate (CRA) in Romania and be at the forefront of groundbreaking medical advancements in a variety of indications (Oncology, Neurology, Gene Therapy...). Key Responsibilities: Monitor Clinical Trials - conduct site visits to ensure compliance with protocols, regulatory requirements and Good Clinical Practice (GCP) Site Management - Serve as the primary point of contact for investigational sites, ensuring smooth study operations. Source Document Verification (SDV) - Review and verify accuracy of clinical data collected from study sites. Investigator Training and Support - Provide ongoing training to site staff on study protocols and regulatory requirements Reporting and Documentation -Prepare monitoring reports, maintain study records, and contribute to overall trial documentation. ​​ Qualifications: Life Sciences University degree or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). ( Fortrea may consider relevant and equivalent experience in lieu of educational requirements) Thorough understanding of ICH GCP Guidelines and u…