About this role
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!
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Learn more about our EEO & Accommodations request here.