Novo Nordisk is seeking a Study Start Up Analyst in Argentina to lead start-up and submission activities for assigned trials, from planning to green light. You will coordinate dossier preparation for Health Authorities and Ethics Committees, ensuring compliance with ICH GCP and local regulations and aligning with Novo Nordisk processes.
You will translate and validate key documents, manage milestones with Trial Managers, and proactively identify risks while supporting inspections and regulatory
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📌 Clinical Trials Start-Up Lead — Regulatory Submissions (Buenos Aires)
🏢 Novo Nordisk A/S
📍 Buenos Aires
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