Revolution Medicines · 8 hours ago
Associate Director, Clinical Development
Redwood City, California, United States
Full-time
Hybrid
Lead/Staff, Director/Executive
$186K/yr - $233K/yr
10+ years expRevolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers. The Associate Director, Clinical Development will contribute to the scientific, clinical, and operational scope of assigned study protocols, leading cross-functional teams in the design, execution, and monitoring of clinical studies.
Health CareLife ScienceMedical
Responsibilities
Develop and execute clinical development strategies and the Clinical Development Plan (CDP) with a focus on early-phase development
Lead cross-functional teams with oversight from senior team members to conduct clinical studies, including study start up, execution and close out activities, data review/analysis, and preparation of study reports
Oversee the development of program-level documents, including but not limited to clinical protocols, investigator’s brochure, clinical study reports, abstracts and manuscripts, presentations, and various other internal and external documents and communications as needed
Conduct ongoing data reviews; prepare and present summaries to internal and external stakeholders
Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and/or individual subject safety
Interact with internal and external stakeholders (investigators, study sites, vendors, committees, etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalation
Conduct literature reviews as needed
Qualification
Required
BS/BA and master's degree in a scientific discipline, or other relevant advanced degree in a health science field
Minimum 10+ years of experience in the pharmaceutical or biotechnology industry as a clinical scientist or related role
Proven leadership in a collaborative team setting and driven by a desire to deploy innovative approaches and technologies in a high-energy environment
Detail-oriented with ability prioritize tasks and function independently as appropriate
Strong organizational skills and an ability to interpret, discuss, and report trial/program level data effectively and identify trends
Proficient with software tools (Microsoft Office), Electronic Data Capture, and other custom web-based software
Excellent written and verbal communication skills
Preferred
Strong experience with clinical data review and data quality assurance
Knowledge and experience with clinical trial management and oversight
Understanding and experience in clinical trial protocol and regulatory document authoring
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
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
Genetic Engineering News
2026-02-02
Pharmaceutical Technology
2026-01-13
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