Intern, Regulatory Affairs

Revolution Medicines • Redwood City, CA

7h • Hybrid

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:
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