Senior Safety Scientist II
Revolution Medicines · Redwood City, CA
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Role summary
Revolution Medicines seeks a Senior Safety Scientist II to provide pharmacovigilance and safety oversight for its oncology portfolio across early and late-phase clinical development. The role involves medical review of safety data, clinical trial protocol assessment, and regulatory document preparation.
What they're looking for
- Advanced degree in life sciences, pharmacy, medicine, or related field
- Demonstrated experience in clinical pharmacovigilance and drug safety assessment
- Knowledge of regulatory requirements for safety reporting and risk management
- Experience with clinical trial protocols, investigator brochures, and safety documentation
- Strong cross-functional collaboration and stakeholder communication skills
- Experience with signal detection and benefit-risk evaluation processes
What you'll be doing
- Conduct proactive safety surveillance of ongoing clinical trials to identify and manage safety signals
- Review and author clinical trial protocols, investigator brochures, informed consent forms, and regulatory safety documents
- Perform medical review of individual case safety reports and routine safety data analysis
- Prepare and present safety data summaries to internal and external stakeholders
- Support regulatory submissions including NDAs, BLAs, and responses to agency safety inquiries
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.