Intern, Regulatory Affairs

Revolution Medicines • Redwood City, CA

4d • $67,000 - $81,000 • Hybrid

About The Position

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: Support regulatory review activities related to site activation across clinical studies. Manage Regulatory Affairs contracts and invoices; maintain and update internal RA tracking tools. Archive regulatory documents in accordance with internal procedures and maintain the regulatory query tracker. Support regulatory submission workflows in Veeva. Co-host Regulatory Sub-Team meetings, including agenda preparation and documentation of action items. Participate in RAxROxMW workshops and Regulatory Strategy Forums. Conduct weekly one-on-one meetings with the RA Manager to review priorities and progress. Build and maintain working knowledge of FDA regulations, guidances, and applicable regulatory requirements.

Requirements

• Currently pursuing a bachelor's degree/MS/PhD in life science, pharmacy, regulatory science, or relevant fields.
• Basic understanding of drug development.
• Attention to detail and organizational skills.
• Must have good verbal and written communication skills.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint).

Nice To Haves

• Familiarity with FDA regulations or global regulatory guidance.
• Prior experience in biotech/pharma or clinical research.

Responsibilities

• Support regulatory review activities related to site activation across clinical studies.
• Manage Regulatory Affairs contracts and invoices; maintain and update internal RA tracking tools.
• Archive regulatory documents in accordance with internal procedures and maintain the regulatory query tracker.
• Support regulatory submission workflows in Veeva.
• Co-host Regulatory Sub-Team meetings, including agenda preparation and documentation of action items.
• Participate in RAxROxMW workshops and Regulatory Strategy Forums.
• Conduct weekly one-on-one meetings with the RA Manager to review priorities and progress.
• Build and maintain working knowledge of FDA regulations, guidances, and applicable regulatory requirements.

What This Job Offers

• Career Level: Intern
• Number of Employees: 251-500 employees