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