Clinical Program Manager
US$164,000 – US$205,000 / yr base salary
Posted 10 Apr 2026
Advertised as “Senior Clinical Program Manager”
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 10+ yrs
- Management level
- People management
- Employment
- Hybrid
| Base salary | US$164,000 – US$205,000 / yr |
|---|
Field of studyBiological Sciences, Health
Study levelBachelor's or higher
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
The Opportunity:
This is a unique opportunity for a Clinical Operations Professional. As a Sr. Clinical Program Manager, you will be responsible for acting as a central contact for the Clinical Study Team(s) and assist with the execution and management of Revolution Medicines (RevMed) clinical trials.
Responsibilities:
-
Adhere to Clinical Standard Operating Procedures (SOP), Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) Guidelines.
-
Be a team leader, providing guidance and oversight for the successful management of all aspects of clinical trials within timelines and designated program budgets.
-
Partner with cross-functional teams to manage, adjust, and revise project timelines and budgets as needed
-
Analyze data health metrics to be shared with stakeholders.
-
Actively partner with cross-functional teams and vendors to drive the query resolution and data listings review process to meet objectives in a timely and efficient process.
-
Conduct risk management, contingency, and scenario planning.
-
Supervise, communicate project status/issues, and problem solve to ensure project team goals are met.
-
Participate in the development of all study-related documentation, including study protocols.
-
Actively contribute in the selection and management of contract research organizations (CROs) and/or vendors, including development of requests for proposals (RFPs).
-
Use all available tools to track, oversee, and communicate on program status to all key stakeholders.
-
Demonstrate the ability to lead and manage multiple complex clinical trials within one or multiple programs with limited oversight.