Merck is seeking an experienced Clinical Research Associate to act as the primary site contact and site manager across all trial phases. You will build strong site relationships, perform on-site monitoring, and ensure regulatory documentation aligns with ICH-GCP and Sponsor SOPs.
You will collaborate with CRA teams and other sponsor functions to achieve Site Ready, participate in site selection, and manage visits and reports in CTMS/eTMF, supporting audits as needed.
📌 Junior CRA: Site Monitoring (Buenos Aires)
🏢 Merck
📍 Buenos Aires
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