Sponsor Dedicated Clinical Research Associate Based in Austria
vor 1 Woche
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.
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