Intern, Regulatory Affairs

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.

Required Skills, Experience and Education:

• 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).

Preferred Skills:

• Familiarity with FDA regulations or global regulatory guidance.

• Prior experience in biotech/pharma or clinical research. 

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