Associate Director, Clinical Development

Revolution Medicines • Redwood City, CA

12h • Hybrid

About The Position

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
The Associate Director, Clinical Development will contribute to the scientific, clinical, and operational scope of assigned study protocols. This role will work with the cross-functional teams for the design, execution, and monitoring of clinical studies, as well as oversee data review, interpretation, and communication to both internal and external stakeholders. Oncology and/or late-stage experience is preferred.

Requirements

• 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.

Nice To Haves

• 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.
• Oncology and/or late-stage experience is preferred.

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Director