Associate Director, Clinical Operations Enablement & Knowledge Systems

Revolution Medicines

Redwood City, California, United States
Not specified; not specified; not specified
**
11+ years direct clinical operations experience
5 years line management experience
6 years cross-functional study management
** Revolution Medicines is seeking an Associate Director of Clinical Operations Enablement & Knowledge Systems to lead the development of a scalable knowledge ecosystem for clinical operations in oncology. The ideal candidate will have extensive experience in clinical operations, strong leadership skills, and a commitment to enhancing study execution quality. **

Job Summary

  • This role is responsible for building and scaling the Clinical Operations knowledge ecosystem to enable consistent, efficient, and high-quality study execution across roles and programs.
  • The ideal candidate combines deep study execution experience with the ability to design scalable, user-centered systems that enable others to perform at their best.
  • The position requires leading organizational change efforts and translating complex clinical workflows into practical tools, guidance, or training materials.

Matching Summary

Match Score: 75

** Revolution Medicines is seeking an Associate Director of Clinical Operations Enablement & Knowledge Systems to lead the development of a scalable knowledge ecosystem for clinical operations in oncology. The ideal candidate will have extensive experience in clinical operations, strong leadership skills, and a commitment to enhancing study execution quality. **

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • 11+ years direct Clinical Operations experience
  • 5 years line management experience
  • 6 years cross-functional study management
  • Strong working knowledge of FDA Regulations ICH Guidelines GCP
  • Experience developing Clinical Operations handbooks and process templates

Nice-to-have

  • Experience deploying AI-enabled solutions
  • Oncology experience in early or late stage trials
  • Familiarity with eTMF EDC IRT CTMS systems
  • Knowledge of Ex-US region clinical trial operations
  • Proficiency in Microsoft Project or Smartsheet

Key Requirements

  • RN or Bachelor's degree in biological sciences or health-related field
  • Minimum 5 years of line management experience
  • Minimum 6 years of cross-functional study management leadership
  • Demonstrated experience building or scaling learning programs within Clinical Operations

Work Rights

Not specified

Tailored Resume

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