Senior Manager, Regulatory Affairs
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 Senior Manager of Regulatory Affairs will provide project teams with regulatory advice, manage, and coordinate various Regulatory Affairs activities within and between departments, and obtain and maintain National Health Authority approvals for investigational products. The position may also undertake regulatory intelligence and research supporting company decision-making. Specifically, you will be responsible for: Manage planning, preparation, coordination, and submission of regulatory documents to global National Health Authorities. Such submissions may include Clinical, Preclinical, or CMC content. Correspond and collaborate with RevMed colleagues and departments to achieve alignment. Function as a Regulatory Affairs subject matter expert member of cross-functional teams, including study teams and submission teams. Perform regulatory research to inform business strategy. Assess and communicate risks. Assure that there are no significant interruptions to the business due to regulatory compliance issues. Collaborates across the organization at all levels, across functional groups, and with executive management. Develop regulatory strategies to inform associated budgets, tools, and specialized support necessary for efficient operations.
Requirements
- Bachelor's Degree in a relevant field and at least 5 years of direct Regulatory experience.
- Strong working knowledge of US FDA Pharmaceutical regulations and guidance.
- Knowledge of EU EMA Pharmaceutical regulations and guidance preferred.
- Proven track record of successful submissions within a regulatory environment.
- Exceptionally strong team player with excellent interpersonal and communication skills.
- Detail-oriented with strong organizational skills and high-quality standards.
Nice To Haves
- Direct experience with oncology drug development highly preferred.
- Experience with combination studies, multiple expansion cohort, basket, or umbrella master protocols highly preferred.
- Direct experience with FDA expedited programs highly preferred.
Responsibilities
- Manage planning, preparation, coordination, and submission of regulatory documents to global National Health Authorities. Such submissions may include Clinical, Preclinical, or CMC content.
- Correspond and collaborate with RevMed colleagues and departments to achieve alignment.
- Function as a Regulatory Affairs subject matter expert member of cross-functional teams, including study teams and submission teams.
- Perform regulatory research to inform business strategy.
- Assess and communicate risks.
- Assure that there are no significant interruptions to the business due to regulatory compliance issues.
- Collaborates across the organization at all levels, across functional groups, and with executive management.
- Develop regulatory strategies to inform associated budgets, tools, and specialized support necessary for efficient operations.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
501-1,000 employees
