Global Study Start-Up Lead: Regulatory Submissions & Access

25 set - Latina
Novo Nordisk Pharma

Novo Nordisk Pharma seeks a qualified professional to drive study start-up processes, enabling timely trial initiation.
You will handle regulatory submissions, coordinate cross-functional teams, and ensure ICH-GCP compliance across projects withinItaly.
The role emphasizes collaboration with local Italian teams, quality documentation, and stakeholder management to accelerate patient access to investigational therapies in a global portfolio.
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