Worldwide Clinical Trials in Argentina is seeking a Regulatory Start-Up Specialist to support end-to-end site activation and maintenance for awarded projects. You will coordinate documents, timelines, and country-specific regulatory needs to help sites activate efficiently.
The role requires at least a two-year life sciences degree, 2+ years in clinical research, and strong organizational skills. English knowledge preferred; multilingualism is a plus.
📌 End-to-End Site Activation (Rincón de los Sauces)
🏢 Worldwide Clinical Trials
📍 Rincón de los Sauces
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