Revolution Medicines · 1 day ago
Senior Clinical Program Manager
Redwood City, California, United States
Full-time
Hybrid
Senior Level, Lead/Staff
$164K/yr - $205K/yr
10+ years expRevolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers. As a Senior Clinical Program Manager, you will act as a central contact for the Clinical Study Team(s) and assist with the execution and management of clinical trials.
Health CareLife ScienceMedical
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
Independently lead Clinical Study Execution Team (CSETs) and influence relevant stakeholders both internally and externally including management
May lead interdepartmental strategic business initiatives as well as spearhead certain SOP development and training
May provide input into strategic and operational short- and long-term therapeutic area development, as appropriate, including supporting alignment and communication to other team members upon implementation
Assists in the hiring, development, and retention of top talent within the team. Coach direct report(s) on their performance, development, and career interests
Participate in other Clinical Operations activities as appropriate
Qualification
Required
RN or Bachelor's or Masters degree in biological sciences or health-related field required
10+ years direct Clinical Operations experience in the pharmaceutical or biotech industry, preferably in Clinical Operations or Clinical Research-related experience. Relevant indirect experiences may also meet the requirement
Minimum of 6 years of cross-functional study management or related leadership experience in life sciences, including multiple years' experience managing project teams
Strong working knowledge of FDA Regulations, ICH Guidelines, and GCP
Proven ability to successfully start-up, manage, and close-out clinical trials, including authoring clinical study and regulatory documentation and SOPs
Experience in selection of CROs/vendors and management of external resources
Thrives in a collaborative team setting that demonstrates flexibility required to maintain a fast pace and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment
Be solution-oriented by anticipating obstacles and difficulties, and proactively providing risk assessment and mitigation strategies to achieve project goals
Excellent written/verbal communication and interpersonal skills
High sense of priority and commitment to excellence in the successful execution of deliverables
Ability to analyze operational data, contribute with a mind on quality, timeliness and fiscal responsibility, make and drive decisions, multi-task, prioritize tasks, anticipate challenges, and execute on goals as a member of an interdisciplinary team
Demonstrate proficiency in Microsoft Office Suite (Outlook, MS Word, Excel, PowerPoint); MS Project and/or Smartsheet a plus
Travel may be required (~25%)
Preferred
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 managing direct reports
Benefits
Competitive cash compensation
Robust equity awards
Strong benefits
Significant learning and development opportunities
Company
Revolution Medicines
Revolution Medicines is an innovative and dynamic organization of expert biologists, chemists, pharmacologists, clinical scientists.
501-1000 employees
H1B Sponsorship
Revolution Medicines has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (13)
2024 (18)
2023 (15)
2022 (8)
2021 (1)
2020 (2)
Funding
Current Stage
Public CompanyTotal Funding
$2.25BKey Investors
Royalty PharmaBoxer CapitalNextech Invest
2025-06-24Post Ipo Debt· $250M
2024-12-02Post Ipo Equity· $750M
2023-03-02Post Ipo Equity· $323.6M
Leadership Team
Luan Wilfong
Chief Human Resources Officer
Steve Kelsey
President
Recent News
2026-01-09
2026-01-09
Company data provided by crunchbase