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Director, U.S. Medical Affairs, Liver Strategy

$243.1k - $314.6k

Gilead

Responsibilities

  • Lead development of USMA Liver strategy for healthcare professional engagement and medical education across PBC and HDV indications
  • Translate strategic priorities into executable medical tactics, materials, congress strategies, and advisory board content
  • Own end-to-end medical resource operations including development oversight, quality standards, and lifecycle management
  • Lead U.S. Medical Review Committee governance and ensure compliance for all liver-related materials
  • Partner cross-functionally with Legal, Regulatory, Commercial, and other teams to drive integrated execution

Requirements

  • Advanced healthcare or scientific degree (MD, PharmD, PhD, or equivalent)
  • 8+ years medical affairs experience in biopharmaceutical industry
  • Leadership experience in strategy and content governance roles
  • Expertise in medical material development and regulatory review processes
  • Strong project management skills across multiple workstreams and timelines
  • Ability to operate in matrixed, cross-functional environment
  • Domestic travel up to approximately 30% including occasional weekends
Vacancy posted a month ago
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