Sponsor Dedicated Cra 2 to Scra Based in Austria

We are seeking a **Sponsor-Dedicated experience CRA** with solid monitoring experience. **Oncology expertise** would be a plus. If you are eager to make an impact, this is your chance! **_This role is for upcoming future opportunities that may arise at Fortrea_** **Key Responsibilities:** In this role, you will * Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements * Build strong relationships with investigators and site staff * Ensure high-quality data collection and patient safety * Work closely with the sponsor, providing insights and updates on study progress * Perform on-site monitoring visits  **Qualifications:** * University or college degree, or certification in a related allied health profession from an appropriately accredited institution (Fortrea may consider relevant and equivalent experience in lieu of educational requirements) * Thorough understanding of ICH GCP Guidelines, of local regulatory requirements and of monitoring procedures. * Basic understanding of the clinical trial process. * Fluent in German and in English, both written and verbal. **What We Offer:** * Competitive salary and performance bonuses * Flexible work arrangements (hybrid /remote options) * Career growth environment in a supportive environment * Works directly with a leading sponsor on innovative studies Ready to take your CRA career to the next level? Apply now! #LI-GQ1 #LI-Remote Learn more about our [EEO & Accommodations request here](https://careers.fortrea.com/us/en/eeo-and-accommodations).