Hybrid Clinical Research Associate: Drive Clinical Trials
CTI Clinical Trial and Consulting Services
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CTI Clinical Trial and Consulting Services seeks a dedicated CRA to act as the primary contact for assigned study sites. You will perform site visits (PSV, SIV, IMV, COV) and ensure timely, compliant deliverables within the Monitoring Plan.
You will also support feasibility, site selection and regulatory document collection. The role requires 3–5 years of CRA experience, a life sciences background, strong ICH-GCP knowledge, and fluent English.
#J-18808-LjbffrOfferta di lavoro pubblicata 2 mesi fa
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