Study Manager, Toxicology
Revolution Medicines · Remote
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Revolution Medicines seeks a Study Manager for Toxicology to oversee non-GLP and GLP toxicology studies from research through clinical development. The role involves managing CRO relationships, coordinating cross-functional activities, ensuring regulatory compliance, and supporting protocol development and submission activities.
What they're looking for
- Bachelor's degree in science discipline
- Minimum 5+ years experience in biotech, pharmaceutical, or CRO environments
- Knowledge of GLP regulations, ICH, and FDA drug development guidelines
- Strong interpersonal and cross-functional collaboration skills
- Effective written and verbal communication abilities
- Ability to prioritize, meet deadlines, and work independently
- Willingness to travel to CRO partner sites as needed
What you'll be doing
- Design toxicology protocols with CROs and internal experts to meet scientific objectives
- Monitor day-to-day study activities for non-GLP and GLP toxicology studies against project goals
- Review protocols, study reports, and amendments with toxicologists for quality assurance
- Coordinate study activities across internal teams and CROs to meet program timelines
- Support regulatory submissions including nonclinical sections of IBs, NDAs, and BLAs
Privacy & handoff
This role links to Revolution Medicines's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.