ICON is a world-leading healthcare intelligence and clinical research organization. The Site Management Associate II will support monitoring and management of clinical trial sites to ensure protocol compliance and GCP adherence.
The role requires strong organizational skills, experience in clinical research, and the ability to collaborate with cross-functional teams while traveling ~25% of the time. ICON is committed to inclusion and delivering high-quality trials.
📌 Clinical Site Management Associate II – Monitoring (Buenos Aires)
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📍 Buenos Aires
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