Clinical Research Associate – Hybrid
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CTI is seeking a Clinical Research professional to serve as the main contact for assigned study sites and to conduct site visits across pre-study, initiation, interim monitoring, and close-out phases in compliance with ICH GCP. You will support start-up activities, site selection, and regulatory document handling while maintaining timelines.
The role requires 3–5 years of CRA experience, including independent monitoring in Germany, a life science background, and fluent English (B2).
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