Senior Medical Director, Solid Tumor Oncology – Strategy

Jazz Pharmaceuticals

Palo Alto (CA)

Remote

USD 308,000 - 462,000

Full time

14 days+
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
401k plan
Paid vacation
Bonus eligibility

Job summary

Jazz Pharmaceuticals is seeking a Senior Medical Director to shape and drive solid tumor oncology medical strategy across development lifecycles. You will provide deep scientific leadership, ensure robust evidence generation, and partner with Clinical Development, Regulatory Affairs, Biostatistics, and Translational Medicine to advance assets.

You will lead integrated development plans, design patient-centric trials, define biomarkers, and represent the company in regulatory discussions with

Qualifications

  • MD or MD/PhD with oncology board certification.
  • 10+ years in oncology clinical or pharmaceutical industry.
  • Leadership in global clinical development and regulatory filings.
  • Track record leading crossfunctional teams in matrixed settings.

Responsibilities

  • Provide strategic medical oversight for solid tumor programs from development to registration and postapproval.
  • Serve as medical authority for assets, ensuring safety, scientific integrity and regulatory compliance.
  • Guide trial design, biomarker strategy, and translational integration.
  • Lead crossfunctional collaboration with Clinical Development, Regulatory Affairs, Biostatistics, and Operations.

Skills

Strategic leadership
Medical leadership
Excellent communication
Stakeholder management
Regulatory familiarity

Education

MD or MD/PhD
Oncology board certification
Advanced clinical training in oncology

Job description

Jazz Pharmaceuticals is seeking a Senior Medical Director to shape and drive solid tumor oncology medical strategy across development lifecycles. You will provide deep scientific leadership, ensure robust evidence generation, and partner with Clinical Development, Regulatory Affairs, Biostatistics, and Translational Medicine to advance assets.

You will lead integrated development plans, design patient-centric trials, define biomarkers, and represent the company in regulatory discussions with

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