Worldwide Clinical Trials in Argentina seeks a subject matter expert and local point of contact for regulatory submissions, site activation, and maintenance for awarded projects. You will plan, initiate, and track documents required for regulatory submissions, and ensure country requirements are met to achieve site activation goals.
You will coordinate with RAM and project teams, review country timelines, communicate risks, and maintain regulatory intelligence.
📌 Regulatory & Site Activation Expert (Buenos Aires)
🏢 Worldwide
📍 Buenos Aires
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