- Location
- Vienna, Austria
- Workplace
- Remote
- Type
- Full-time
- Source
- Workday
Description
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.
