Clinical Research Associate Sponsor Dedicated in Austria
vor 1 Woche
We are seeking a **Sponsor-Dedicated CRA** with solid monitoring experience. If you are eager to make an impact, this is your chance
**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
LI-GQ1 #LI-Remote
Learn more about our EEO & Accommodations request here.
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