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Monitoring clinical trial sites across Argentina to ensure compliance with ICH-GCP guidelines, study protocols, and regulatory requirements
Conducting site initiation, routine monitoring, and close-out visits at investigator sites
Reviewing and verifying source documents, ensuring data quality and integrity for submission to regulatory authorities
Building strong relationships with principal investigators, study coordinators, and site staff to support successful trial execution
Managing eTMF documentation and IVRS systems, ensuring accurate and timely data entry
Identifying and resolving site-level issues proactively, escalating when necessary
Traveling within Argentina approximately twice per month to visit clinical trial sites
Clinical Research Associate - Talent Pipeline
Vicente Lopez, Buenos AiresPosted 1 weeks ago