Novo Nordisk Italy is seeking a Senior Study Start-up Specialist to enable clinical trials to launch on time and in compliance with local and international regulations. You will manage end-to-end study start-up, navigating regulatory landscapes to ensure sites are activated efficiently and patients access investigational treatments quickly.
You will oversee regulatory authority and ethics submissions, coordinate start-up documents through CTIS portal, ensure ICH-GCP compliance, and collaborate
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📌 Senior Study Start-Up Lead (Latina)
🏢 Biopharma Careers
📍 Latina
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