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
- 80 days Revolution Medicines's roles stay open a median of 78 days
- Reposted
- No
- Salary listed
- No 0% of Revolution Medicines's roles list one
- Ghost-job risk at Revolution Medicines
- high 259 stale, 6 reposted of 264 open
- Hiring momentum
- 449 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-10-22
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.
- 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 2026-10-22. PitchMeAI is not the employer.
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