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.
📌 Global Study Start-Up Lead: Regulatory Submissions (Italia)
🏢 Altro
📍 Italia