Strategic Medical Lead, Multiple Myeloma

1110 Kite Pharma, Inc.

Foster City (CA)

On-site

USD 196,000 - 253,000

Full time

14 days+

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Benefits offered by this job

Discretionary bonus
Stock-based incentives
Paid time off
Benefits package

Job summary

Kite Pharma, Inc. is seeking an Associate Director, Multiple Myeloma to join the U.S. Medical Affairs team and advance medical strategy, evidence generation, and launch readiness across the myeloma portfolio.

This role focuses on translating data into actionable medical initiatives and cross-functional collaboration. You will partner with Field Medical, Commercial, Market Access, HEOR/RWE, Clinical Development, Regulatory, Safety, and Global Medical Affairs, reporting to the U.S.

Responsibilities

  • Independently lead priority workstreams while contributing to the development and execution of the U.S. Multiple Myeloma Medical Affairs strategy.
  • Serve as a strategic medical partner to Field Medical, Commercial, Market Access, HEOR/RWE, Clinical Development, Regulatory, Safety, and Global Medical Affairs teams.
  • Translate clinical data, treatment landscape insights, competitive intelligence, and stakeholder feedback into actionable medical strategies and evidence-generation opportunities.
  • Support the development and refinement of scientific communication platforms, core medical content, FAQs, presentations, and field-facing resources that enable compliant scientific exchange.
  • Lead or support advisory boards, expert engagement activities, congress initiatives, symposia, medical education programs, and stakeholder events aligned with medical objectives.

Job description

Kite Pharma, Inc. is seeking an Associate Director, Multiple Myeloma to join the U.S. Medical Affairs team and advance medical strategy, evidence generation, and launch readiness across the myeloma portfolio.

This role focuses on translating data into actionable medical initiatives and cross-functional collaboration. You will partner with Field Medical, Commercial, Market Access, HEOR/RWE, Clinical Development, Regulatory, Safety, and Global Medical Affairs, reporting to the U.S.

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