Make a meaningful impact in clinical research by joining our sponsor-dedicated team as a Clinical Research Associate (CRA). This role offers the opportunity to monitor sites in Austria and in Switzerland, while working on cutting-edge studies that shape the future of healthcare.
Key Responsibilities:
- Identify and assess new potential investigators and sites.
- Recommend sites during feasibility and selection phases.
- Conduct pre-study, initiation, monitoring, and close-out visits.
- Monitor site performance, data quality, and protocol compliance.
- Act as a key point of contact for site personnel, providing training and support.
- Use data insights to assess risks and drive decisions.
- Support regulatory audits, EC submissions, and system access coordination.
Required Qualifications :
- University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
- Basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations governing clinical trials.
- Solid understanding of clinical research processes, regulations, and methodology.
- Strong organizational and time management skills.
- Ability to build and maintain relationships
- 1 to 3 years of monitoring experience required within CRO or Pharma environment.
Why Join Us?
- Be part of a sponsor-dedicated team with a strong pipeline and purpose.
- Enjoy regional monitoring—minimizing travel while maximizing your impact.
- Collaborate with passionate professionals in a supportive environment.
- Contribute to meaningful research that improves lives.
We invite qualified candidates who are committed to excellence in clinical research to apply and become part of Fortrea’s mission to advance healthcare worldwide. If you are seeking a rewarding opportunity within a globally respected organization, we encourage you to submit your application today.
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Learn more about our EEO & Accommodations request here.
Skills Required
- University or college degree in life sciences, nursing, pharmacy, or a related allied health profession, or equivalent relevant experience
- Basic to good knowledge of ICH/GCP Guidelines and applicable local clinical trial laws and regulations
- Solid understanding of clinical research processes, regulations, and methodology
- Strong organizational and time management skills
- Ability to build and maintain professional relationships
- One to three years of monitoring experience in a CRO or pharmaceutical environment
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
