Executive Director, GCP QA (Good Clinical Practice, Quality Assurance)

Revolution Medicines · Redwood City, California, United States

Posted
1 day ago
Last confirmed live
Today

What this role involves

This is a senior leadership role responsible for global GCP quality strategy across clinical development programs, ensuring compliance with regulatory requirements and industry standards. The Executive Director oversees GCP QA activities, including audit/inspection readiness, vendor management, and continuous improvement. They represent QA in cross-functional and executive forums and report to the Vice President of Global Quality.

Skills this posting asks for

  • good clinical practice
  • quality assurance
  • glp
  • pharmacovigilance
  • regulatory compliance
  • ich guidelines
  • fda regulations
  • ema regulations
  • risk-based quality management
  • trial master file
  • gxp computerized systems
  • data integrity
  • auditing
  • inspection readiness
  • corrective and preventive actions
  • vendor management
  • cro management
  • key performance indicators
  • clinical development
  • oncology

Requirements

  • Level: director

From the employer’s posting

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is adv…

Read the full description on Revolution Medicines’s careers page

Apply without filling the form

Approve this role and the application is completed for you, including a résumé tailored to it. You get a confirmation when it lands, and a credit is only spent when a submission is confirmed.

Other roles at Revolution Medicines

All 53 roles at Revolution Medicines