VP, Cancer Vaccines Medicine Development Leader (Global)

GSK

Upper Providence (Delaware County)

Hybrid

USD 341,000 - 568,000

Full time

7 days ago
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Job summary

GSK in Cambridge, MA/Stevenage has a VP-level role overseeing the global development of a cancer vaccine from early development through approval and launch. The position requires leading a matrix MDT across clinical development, translational medicine, safety, regulatory, medical affairs and manufacturing, with on-site presence required two days per week.

The role emphasizes strategic vision within Oncology R&D, portfolio prioritization and interaction with senior leadership and external

Qualifications

  • Advanced degree including MD, PhD, PharmD, MBA, or MS in a relevant field.
  • Experience leading development and registration of medicines, especially cancer vaccines or immuno-oncology.
  • Filing experience with BLA/NDA/MAA submissions as a core responsibility.
  • Experience across R&D to commercialization, including regulatory and manufacturing.
  • Leadership in a complex, global matrix organization with high accountability.

Responsibilities

  • Act as single point of accountability for global development of a cancer vaccine asset.
  • Lead the Medicine Development Team across clinical, regulatory, safety and manufacturing areas.
  • Align asset strategy with Oncology R&D and drive lifecycle management.
  • Collaborate with internal and external stakeholders to enable successful regulatory approvals.
  • Oversee resource planning, budget management and strategic investments.

Skills

Medicines development leadership
Oncology vaccine knowledge
Immuno-oncology experience
Regulatory submissions (BLA/NDA/MAA)
Global development with matrix teams
P&L and budget management

Education

MD/PhD/PharmD/MBA/MS Oncology drug development expertise

Job description

GSK in Cambridge, MA/Stevenage has a VP-level role overseeing the global development of a cancer vaccine from early development through approval and launch. The position requires leading a matrix MDT across clinical development, translational medicine, safety, regulatory, medical affairs and manufacturing, with on-site presence required two days per week.

The role emphasizes strategic vision within Oncology R&D, portfolio prioritization and interaction with senior leadership and external

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