About the job
Join Revolution Medicines, a pioneering clinical-stage precision oncology company dedicated to the development of innovative targeted therapies aimed at inhibiting cutting-edge targets in RAS-addicted cancers. Our research and development pipeline features RAS(ON) Inhibitors designed to suppress a variety of oncogenic RAS protein variants, as well as RAS Companion Inhibitors for combination treatment strategies. As a new member of our team, you will collaborate with exceptional colleagues committed to transforming the lives of patients with cancers influenced by mutations in the RAS signaling pathway.
The Opportunity:
The Manager of Regulatory Affairs will play a pivotal role by providing regulatory guidance to project teams, managing and coordinating various Regulatory Affairs activities across departments, and securing and maintaining approvals from National Health Authorities for investigational products. Additionally, this role will involve conducting regulatory intelligence and research to support strategic decision-making within the company.
Oversee the planning, preparation, coordination, and submission of regulatory documents to global National Health Authorities, including Clinical, Preclinical, or CMC content.
Collaborate effectively with Revolution Medicines colleagues across departments to ensure alignment.
Serve as a Regulatory Affairs subject matter expert in cross-functional teams, including study and submission teams.
Conduct regulatory research to inform business strategies and communicate associated risks.
Ensure continuity of business operations by mitigating regulatory compliance issues.
Engage with all levels of the organization, including executive management, to foster collaboration.
Develop regulatory strategies that inform budgeting and resource allocation to enhance operational efficiency.

