Senior Director, Global Patient Safety Science

Revolution Medicines

Redwood City, California, United States
Base pyy range determined by role, level, + locati...
On-site
10+ years drug development experience
6+ years safety science experience
Medical review of icsrs and safety data
Revolution Medicines is seeking a Senior Director of Global Patient Safety Science to oversee safety science and pharmacovigilance across their oncology product portfolio. The ideal candidate will have extensive experience in drug development and safety science, and will be responsible for safety oversight and risk management activities

Job Summary

  • The Senior Director will provide safety oversight and input into all aspects of study management across the RevMed portfolio.
  • This role is accountable for the benefit/risk safety profile of allocated products throughout the product lifecycle.
  • The position requires leading representative interactions with Health Authorities during scientific advice forums and meetings.

Matching Summary

Match Score: 85

Revolution Medicines is seeking a Senior Director of Global Patient Safety Science to oversee safety science and pharmacovigilance across their oncology product portfolio. The ideal candidate will have extensive experience in drug development and safety science, and will be responsible for safety oversight and risk management activities.

Salary

Base pay range determined by role, level, and location; includes competitive cash compensation; robust equity awards included

Skills & Requirements

Must-have

  • 10+ years drug development experience
  • 6+ years Safety Science experience
  • Medical review of ICSRs and safety data
  • Safety surveillance and signal detection
  • Risk management strategy development
  • Regulatory submission preparation
  • Postgraduate qualification in Life Sciences

Nice-to-have

  • 4+ years Oncology clinical development
  • BLA/MAA regulatory interaction experience
  • Global matrix environment leadership
  • Strong emotional intelligence
  • Mentoring high-performing teams
  • Data Monitoring Committee participation

Key Requirements

  • MD, PharmD, PhD/MSc or equivalent postgraduate degree
  • Minimum 10 years total drug development experience
  • At least 6 years specific Safety Science experience
  • Experience leading Regulatory Authority meetings (FDA/EMA)

Work Rights

Not specified

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