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The Clinical Research Associate will conduct site monitoring visits, including initiation and close-out, to ensure protocol compliance and data quality. They will also act as the primary point of contact for site personnel and support regulatory submissions and risk assessment activities.
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:
Required Qualifications :
Why Join Us?
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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