ICON is a general healthcare intelligence and clinical research organisation. The Clinical Site Associate will support site management activities and ensure trials are conducted efficiently, compliantly, and to high quality standards.
You will assist with site activation, document collection, and maintaining trackers, while coordinating site visits and ensuring audit readiness. Travel about 10% may be required in support of trial sites.
📌 Hybrid Clinical Site Lead – Global Research (Quilmes)
🏢 Mercor
📍 Quilmes
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