Global Program Manager biologics phase III

Global Program Manager biologics phase III

My client is an innovating, dynamic and growing international pharmaceutical company currently expanding their regulatory team in Switzerland, Vaud Canton.

Due to this growth my client is looking for a Senior Global Program Manager (expert in phase III and biological products) to provide day-to-day project management leadership to global drug development project teams. He/she will maintain project plans and budgets, organize and lead project team meetings to meet goals


  • Bring strong expertise with biological product development plans
  • Coordinates global, cross-functional, complex drug development project teams and provides advanced project management support, including action item tracking, organization and communication of materials.
  • Organizes interdepartmental activities to ensure completion of assigned projects within scope, on schedule and within budget constraints.
  • Identifies, monitors, and analyzes business project risks and prepares project planning contingency scenarios.
  • Ensures accurate tracking and reporting of project milestones and deliverables
  • Identifies and communicates resource constraints to senior management.
  • Prepares project updates for governance meetings and clearly communicates status in written documents and presentations.
  • Ensures documentation of, and access to, key project documents, presentations and data.
  • Assumes full responsibility for managing specific aspects of the project as designated by team leadership
  •  Bring a strong expertise with CMC aspects and market access.

Expected qualifications:

  • Bachelor or PhD degree (MBA)
  • At least ten years of relevant experience in experience in a Biopharma or Biotech environment with and seven years in a similar position in Project Management
  • Strong expertise in managing phase III and biological product.
  • Thorough understanding of the drug development processes
  • Hands-on expertise with project management tools (knowledge of Planiswere program will be a plus)
  • Ability to work on a Senior / Strategic level
  • Good understanding of financial and resource planning systems and processes and ability to coordinate project level budget/resource estimates and manage actuals vs. plan
  • Good experience with regulatory aspect (CMC) and market access
  • Good communication
  • Fluent in English

For more details, please contact Marine Dollat at

Marine Dollat

Specialist Pharmaceutical and Medical Device recruiter and headhunter recruiting in Switzerland and France for the provision of Pharma and Medical Device staff including Quality (GCP, GMP, GLP, GxP, Quality System, Quality Engineer, Quality manager, Quality director and VP level), Regulatory Affairs or Production's position. As specialists in the placement of candidates within the Pharmaceutical Industry, our service is thorough, professional and intelligent. In addition to our permanent and contract recruitment services, we provide proactive search campaigns, advertising campaigns and dedicated account management. If you would like to have a confidential discussion regarding your search for staff or your search for a new position please feel free to contact me directly at