About this role
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 :
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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.
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Basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations governing clinical trials.
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Solid understanding of clinical research processes, regulations, and methodology.
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Strong organizational and time management skills.
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Ability to build and maintain relationships
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1 to 3 years of monitoring experience required within CRO or Pharma environment.
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Why Join Us?
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Be part of a sponsor-dedicated team with a strong pipeline and purpose.
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Enjoy regional monitoring—minimizing travel while maximizing your impact.
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Collaborate with passionate professionals in a supportive environment.
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Contribute to meaningful research that improves lives.
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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.