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Clinical Program Manager

Revolution Medicines
Location
Redwood City, California, United States
Posted
17 days ago
Department
Clinical Operations
What they actually want (must-haves)
  • RN or Bachelor’s or Masters degree in biological sciences or health-related field
  • 8+ years direct Clinical Operations experience in the pharmaceutical or biotech industry
  • Minimum of 4 years of cross-functional study management or related leadership experience in life sciences
  • Strong working knowledge of FDA Regulations, ICH Guidelines, and GCP
  • Proven ability to successfully start-up, manage, and close-out clinical trials
  • Experience in selection of CROs/vendors and management of external resources
Nice to have
  • Familiarity working with vendor systems/portals (e.g., eTMF, EDC, IRT, CTMS)
  • Oncology experience, early and/or late stage, strongly preferred
  • Knowledge and/or familiarity with Ex-US region(s) clinical trial operations
  • Some experience mentoring junior staff
What the job really is

As a Clinical Program Manager at Revolution Medicines, you will oversee the execution and management of clinical trials, acting as the central contact for the Clinical Study Team. Your responsibilities include adhering to clinical standards, managing timelines and budgets, analyzing data metrics, and collaborating with cross-functional teams and vendors. You will also participate in study documentation development and mentor junior team members while leading complex trials with minimal oversight.

Benefits
  • Base pay salary range of $143,000 — $178,000 USD
  • Competitive cash compensation
  • Robust equity awards
  • Strong benefits
  • Significant learning and development opportunities
Things to weigh
  • Travel may be required (~25%)
  • Role involves leading complex trials with some oversight
  • No specific mention of remote work flexibility, but hybrid work is indicated
Job score3.2/5
Benefits3/5
Freshness4/5
Career value4/5
Role clarity5/5
Pay transparency0/5

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