Global GI Cancer Medical Director - Remote Leadership

Jazz Pharmaceuticals, Inc.

Philadelphia (Philadelphia County)

Remote

USD 268,000 - 402,000

Full time

8 days ago

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Benefits offered by this job

Medical insurance
401k retirement plan
Paid time off

Job summary

Jazz Pharmaceuticals, Inc. is seeking a Senior Global Medical Director, Gastrointestinal Cancers to lead medical affairs in a global context.

The role focuses on aligning regional needs with global R&D and commercial priorities, guiding evidence strategies and publication plans, and influencing development decisions across regions. You will collaborate across Medical Affairs, Clinical Development, Regulatory, and Market Access to ensure timely, scientifically sound decisions that benefit

Qualifications

  • Minimum 10 years in Medical Affairs, Clinical Development, or related pharma industry experience, oncology preferred.
  • Experience in GI cancers and/or HER2-targeted therapies strongly preferred.
  • Proven ability to develop and execute evidence-generation strategies and publication plans.
  • Strong understanding of oncology drug development and external scientific engagement.

Responsibilities

  • Lead the GI Cancer Global Medical functional matrix team.
  • Partner with US and EUR/INT Medical Affairs to align regional needs and priorities.
  • Represent medical perspectives within global cross-functional governance (CDT, LDT, PGC, DPRC).
  • Inform early development activities with regional insights for TPP and trial design.
  • Oversee evidence-generation activities and lifecycle planning across regions.

Skills

Medical affairs
Clinical development
Evidence generation
Publications strategy
Stakeholder management
Strategic thinking
Cross-functional collaboration

Education

Advanced degree
PharmD/PhD/MD

Job description

Jazz Pharmaceuticals, Inc. is seeking a Senior Global Medical Director, Gastrointestinal Cancers to lead medical affairs in a global context.

The role focuses on aligning regional needs with global R&D and commercial priorities, guiding evidence strategies and publication plans, and influencing development decisions across regions. You will collaborate across Medical Affairs, Clinical Development, Regulatory, and Market Access to ensure timely, scientifically sound decisions that benefit

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