As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
We are seeking a Sponsor-Dedicated CRA with solid monitoring experience to be part of a clinical trial in Medical Device/Diabetes. If you are eager to make an impact, this you chance!

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

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

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