Consultant – Regulatory Affairs Project Manager

Il y a 2 jours

Paris, Nouvelle-Aquitaine, France Ividata Life Sciences Temps plein 90 000 € - 130 000 € Contrat
  • Lead the execution of the global submission plan across the entire product lifecycle
  • Anticipate operational risks and manage planning and timelines
  • Structure the dossier hierarchy and coordinate the collection of documents
  • Oversee publishing vendors and coordinate the preparation of responses to health authority queries

Requirements

  • Minimum 10 years' experience in project management within a demanding Regulatory Affairs environment
  • Strong knowledge of eCTD dossiers and international submission processes
  • Fluent English