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Revolution Medicines

Associate Director, Global Regulatory Affairs Project Management

Revolution Medicines · Redwood City, California, United States

Posted about 3 months ago

or apply directly on Revolution Medicines's site. We never take the application ourselves.

Is this posting real?

This role has been open
102 days
Revolution Medicines's roles stay open a median of 101 days
Reposted
No
Salary listed
No
0% of Revolution Medicines's roles list one
Ghost-job risk at Revolution Medicines
high
264 stale, 6 reposted of 264 open
Hiring momentum
88 roles opened in the last 90 days
↓ down vs. the prior 90 days
Last confirmed on the employer's board
2026-11-14

Measured from postings appearing on and disappearing from Revolution Medicines's own greenhouse board since 2026-08-03. Full hiring picture for Revolution Medicines.

About this role

The Associate Director, Global Regulatory Affairs Project Management at Revolution Medicines will lead the execution of global regulatory strategies for oncology drug marketing applications. This role involves project management of regulatory submissions, collaboration with cross-functional teams, and ensuring timely delivery of high-quality regulatory deliverables. The position requires a strong understanding of oncology drug development and regulatory processes, along with exceptional project management skills.

Our read on this posting2.6out of 5
benefits
3/5
freshness
1/5
career value
4/5
role clarity
5/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Revolution Medicines as an employer.

What you need

  • Bachelor’s degree in life sciences or related discipline; advanced degree preferred
  • 12+ years of pharma/biotech industry experience
  • 6-8+ years of regulatory project management experience
  • Hands-on U.S. drug marketing application experience
  • Strong working knowledge of global regulatory regulations and submission pathways
  • In-depth knowledge of CTD structure and dossier component management

Nice to have

  • Experience supporting global regulatory filings including Japan, Canada, and EU/UK submissions
  • Oncology drug development experience
  • Experience with complex oncology clinical trial designs

What you get

  • Base pay salary range of $177,000 — $221,000 USD
  • Competitive cash compensation
  • Robust equity awards
  • Strong benefits
  • Significant learning and development opportunities

Worth weighing

  • No specific mention of remote work options, but hybrid work is indicated
  • Base pay salary range is dependent on multiple factors
  • No detailed information on the company's culture or work environment provided

Summarised from Revolution Medicines's posting. Read the full original.

Listed by Revolution Medicines on their greenhouse job board, last confirmed open on 2026-11-14. PitchMeAI is not the employer.

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