Senior Manager, Regulatory Affairs at Revolution Medicines

You're a seasoned regulatory affairs professional with at least five years of experience and a Bachelor's degree in a relevant field. You have a solid understan

Work type: hybrid

Location: Redwood City, California, United States

Salary: $164,000 – $205,000/yr

Type: Full-time

Summary

You're a seasoned regulatory affairs professional with at least five years of experience and a Bachelor's degree in a relevant field. You have a solid understanding of US FDA pharmaceutical regulations and a track record of successful submissions. **What makes it worth a look...** This full-time, hybrid role at Revolution Medicines in Redwood City, California, offers a competitive salary range of $164,000 - $205,000 per year. You'll be part of a company developing novel targeted therapies for cancer. **You might be a good fit if you...** * Possess strong working knowledge of US FDA pharmaceutical regulations and guidance. * Have direct experience with IND/NDA filings. * Can manage and coordinate regulatory affairs activities and submissions. * Are adept at assessing and communicating regulatory risks.

Job Description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. 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.

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.








Required Skills, Experience and Education:






Preferred Skills:



#LI-Hybrid #LI-SH1

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

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