Medical Director

Revolution Medicines • Redwood City, CA

258d • $273,000 - $342,000

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 professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. Revolution Medicines Medical Directors are responsible for formulating clinical development strategy and ensuring effective execution of this plan for the assigned molecule(s)/combination(s)/indication(s). Revolution Medicines has a robust research pipeline from discovery to clinic, and we are working rigorously to leverage this for the greatest possible impact for patients. As a clinician and scientist, you will be bridging the basic research with clinical development strategy in this scientifically rich environment.

Requirements

• M.D. with clinical training.
• Minimum 4 years’ experience in pharma/biotech clinical development.
• Experience working with the principles and techniques of data analysis, interpretation, and clinical relevance.
• Excellent judgment and decision-making skills with outstanding attention to detail.
• Curiosity and a strong drive to grow.
• Strong written / verbal communication with good interpersonal and influencing skills.
• Excellent project management skills. Ability to prioritize multiple tasks and goals to ensure their timely and effective completion.

Nice To Haves

• Recognized expert in the field.
• Academic/teaching background a plus.
• Prior medical monitoring experience.
• Phase III experience as medical monitor or clinical scientist.
• Option to travel globally for conferences (<15%).

Responsibilities

• Maintains the highest standards of scientific and clinical knowledge in the specific therapeutic area(s) of assignment.
• Stays informed and up to date of internal and external developments, trends, and other dynamics relevant to the clinical development plan, and maintains a current view of the relevant disease area(s) to inform strategy.
• Collaborates with external stakeholders such as clinical investigators and scientists.
• Participates in the Clinical Development Steering Team to review, discuss, and provide clinical and scientific input regarding early clinical development plans company/portfolio wide.
• Works with external investigators to advise on and evaluate Investigator Sponsored Trials.
• Provides the clinical and expert input in the development of clinical sections of Investigator Brochures, presentations, and other materials.
• Engages regularly with relevant external investigators and participates in the identification and selection of appropriate external investigators and sites.
• Acts as the medical monitor for assigned studies.
• Conducts ongoing reviews of clinical trial data with a focus on medical related items.
• Collaborates within a multidisciplinary team including biostatisticians to develop study analytics and data review plans.
• Collaborates with the Translational Medicine team to strategize, design, and implement biomarker plans.
• Reviews study data to ensure correct medical/scientific data interpretation for interim and final study reporting.
• Collaborates with Clinical Operations for site selection, feasibility, and query resolution etc.
• Collaborates with relevant team members to support regulatory interactions such as end of phase meetings.

Benefits

• Competitive cash compensation.
• Robust equity awards.
• Strong benefits.
• Significant learning and development opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Master's degree