Global Study Start-Up Lead: Regulatory Submissions & Access

27 set - Provincia di Latina
Novo Nordisk Pharma

Novo Nordisk Pharma seeks a qualified professional to drive study start-up processes, enabling timely trial initiation.L'esperienza richiesta ai candidati, così come le competenze e le qualifiche aggiuntive necessarie per questo lavoro, sono elencate di seguito.You will handle regulatory submissions, coordinate cross-functional teams, and ensure ICH-GCP compliance across projects withinItaly. xysqume The role emphasizes collaboration with local Italian teams, quality documentation, and stakeholder management to accelerate patient access to investigational therapies in a global portfolio.#J-18808-Ljbffr

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