Director, Global Names Patient Access Strategy & Operations

Scorpion Therapeutics

United States

Remote

USD 180,000 - 280,000

Full time

14 days+
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Job summary

Revolution Medicines seeks a leader to direct global strategy and operations for charged-for named patient access to its investigational oncology therapies, focusing on compliant, physician-initiated importation pre-regulatory approval.

You will collaborate with cross-functional teams (Supply Chain, Medical Affairs, Legal, Regulatory, IT), manage vendor relationships, and secure governance approvals while ensuring adherence to policies and regulations.

Qualifications

  • Bachelor's in healthcare with 8–10+ years biotech/pharma experience.
  • Proven success in global early access programs.
  • Strong regulatory knowledge.
  • Outstanding project management.
  • Cross-functional leadership skills.

Responsibilities

  • Develop and implement global access initiatives.
  • Oversee operational execution.
  • Collaborate with cross-functional teams (Supply Chain, Medical Affairs, Legal, Regulatory, IT).
  • Manage vendor relationships.
  • Secure governance approvals.
  • Ensure adherence to policies and regulations.

Skills

Global access strategy
Cross-functional leadership
Regulatory knowledge
Vendor management
Program management

Education

Bachelor's in healthcare

Job description

Role

Lead global strategy and operations for charged-for named patient access of Revolution Medicines’ investigational oncology therapies, focusing on compliant, physician-initiated patient importation pre-regulatory approval.

Responsibilities
  • develop and implement global access initiatives
  • oversee operational execution
  • collaborate with cross-functional teams (Supply Chain, Medical Affairs, Legal, Regulatory, IT)
  • manage vendor relationships
  • secure governance approvals
  • ensure adherence to policies and regulations.
Qualifications
  • Bachelor's in healthcare with 8-10+ years of biotech/pharma experience
  • proven success in global early access programs
  • strong regulatory knowledge
  • outstanding project management
  • cross-functional leadership skills.
HighValue
  • oncology
  • early access programs
  • global regulatory considerations
  • physician-led importation
  • cross-functional stakeholder engagement
  • experience in small or large biotech firms
  • ability to operate in a fast-growth environment.
WorkSetup
  • remote, based in Redwood City, CA
  • no specific travel requirements stated.
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