CTI is seeking a Clinical Research Associate (CRA) to serve as primary CTI contact for assigned study sites, conduct site visits (PSV, SIV, IMV, COV) and ensure monitoring deliverables meet ICH-GCP and regulatory requirements.
You will support start-up activities, maintain essential regulatory documents, track subject status, and collaborate with project teams. Fluent English (B2) and a life-science background are required; hybrid work opportunities offered.
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