Global Study Start-Up Lead – Regulatory & Ethics

Novo Nordisk A/S in Italy is seeking a Senior Study Start-up Specialist to drive regulatory submissions and site activation for clinical trials, ensuring compliance with ICH-GCP and local requirements. You will manage end-to-end start-up, coordinate with internal and external stakeholders, maintain trial master file, and support contracts and budgets in a fast-paced, global environment. Joining the Clinical Development Centre (CDC) in Trial Operations EUCAN, you will contribute to timely trial

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