Cra 2 - 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 understanding of **local regulatory requirements**. * Thorough **knowledge of monitoring procedures** and basic understanding of the clinical trial process. * **Fluency in Romanian and in English**, both written and verbal. **What We Offer:** * Flexible work arrangements (hybrid /remote options) * Career growth environment in a supportive environment * Dedicated Line Manager * Works directly with a leading sponsor on innovative studies * Attractive salary and Fortrea benefits If you are passionate about clinical research, thrive in a collaborative environment, and seek exciting career growth, we want to hear from you! #LI-Remote #LI-Hybrid Learn more about our [EEO & Accommodations request here](https://careers.fortrea.com/us/en/eeo-and-accommodations).