Clinical Trials Manager
Revolution Medicines · Redwood City, CA
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 an experienced Clinical Trials Manager to oversee Phase I-III oncology studies in a commercial setting. The role involves managing contract research organizations, ensuring regulatory compliance, coordinating clinical study execution, and collaborating across functional teams to advance the company's RAS-targeted cancer pipeline.
What they're looking for
- Phase I-III clinical trial management experience in industry setting
- Strong knowledge of Good Clinical Practice (GCP) and FDA regulatory requirements
- Oncology clinical operations experience preferred
- Contract Research Organization (CRO) oversight and vendor management expertise
- Familiarity with International Council for Harmonization (ICH) guidelines
- Site assessment, investigator qualification, and monitoring experience
What you'll be doing
- Oversee CRO activities and clinical study execution to meet timelines, budgets, and regulatory compliance
- Identify, engage, and manage clinical vendors including CROs, core labs, and EDC providers
- Conduct site visits including training, initiation, and monitoring activities
- Collaborate with internal teams across clinical development, regulatory, QA, and finance functions
- Review study documentation, monitoring reports, and assist with safety and clinical study reports
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.