Global Study Start-Up Lead: Regulatory Submissions & Access
Novo Nordisk Pharma
pNovo 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. /ppThe role emphasizes collaboration with local Italian teams, quality documentation, and stakeholder management to accelerate patient access to investigational therapies in a global portfolio. /p #J-18808-Ljbffr
Offerta di lavoro pubblicata 2 giorni fa
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