Associate Director, Clinical Quality
Revolution MedicinesRedwood City, California, United States
Posted September 26, 2025
180000 - 225000 USD year
Full Time
About the Company
Revolution Medicines is dedicated to discovering, developing, and delivering innovative targeted medicines for cancer patients. The company focuses on RAS-addicted cancers, which represent 30 percent of new human cancer diagnoses. Revolutionaries work tirelessly to develop cutting-edge therapeutic approaches, setting them apart in the industry with their commitment to tackling some of the toughest cancers.
Job Description
Revolution Medicines is seeking an Associate Director, Clinical Quality Assurance to support clinical trials and ensure regulatory compliance for their precision oncology products. This role involves leading and supporting GCP compliance, collaboration with clinical and external teams, and providing risk-based quality management. The ideal candidate will contribute to a culture of quality and open communication.
Requirements
- Bachelor’s degree in scientific or technical discipline.
- 8 years of experience in GCP Quality in the pharmaceutical or biotechnology industry.
- 8 years in any of the following areas: audit or audit management experience, inspection readiness, Deviation/CAPA management, or related quality management system responsibilities.
- Extensive knowledge of ICH GCP and other relevant regulatory requirements.
Benefits
- Competitive cash compensation
- Robust equity awards
- Strong benefits
- Significant learning and development opportunities
