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.