This may be time for you to join our innovative FSP team as a Clinical Research Associate (CRA) in Austria 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 tranining 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 German 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-GQ1 #LI-Remote #LI-Hybrid

Learn more about our EEO & Accommodations request here.