Director, Regulatory Operations, Systems
Revolution Medicines · Redwood City, California, United States
Posted 15 days ago
or apply directly on Revolution Medicines's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 15 days Revolution Medicines's roles stay open a median of 43 days
- Reposted
- No
- Salary listed
- No 0% of Revolution Medicines's roles list one
- Ghost-job risk at Revolution Medicines
- low 0 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
- 2026-09-17
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 Director of Regulatory Operations at Revolution Medicines will lead the development and optimization of the company's regulatory information management capabilities, primarily focusing on the Veeva Vault RIM platform. This role involves strategic leadership, overseeing system management, and ensuring compliance with global regulatory submission requirements. The director will also collaborate with various departments to enhance processes and drive innovation in regulatory data management.
- benefits
- 3/5
- freshness
- 4/5
- 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 a life science, technical, or related field
- 12+ years of experience in the biotechnology, pharmaceutical, or medical device industry
- 3–5 years focused on Regulatory Affairs/Operations and Veeva RIM systems
- Experience with submission management in EU, Japan, and Canada
- Proven leadership experience, including building functions and managing teams
- Strong understanding of global regulatory submission requirements
Nice to have
- Advanced knowledge of Veeva Vault RIM and related regulatory systems
- Experience supporting oncology drug development and regulatory submissions across the full product lifecycle
- Familiarity with structured data submissions, including Veeva Registrations and IDMP readiness
- Prior experience in digital transformation initiatives
- International experience with global submissions and regional regulatory requirements
What you get
- Base pay salary range of $211,000 — $264,000 USD
- Competitive cash compensation
- Robust equity awards
- Strong benefits
- Significant learning and development opportunities
Worth weighing
- Role involves building and scaling a new function, which may present challenges
- Focus on Veeva Vault RIM platform may limit exposure to other systems
- Requires collaboration across multiple departments, which can be complex
- No specific mention of remote work flexibility despite hybrid designation
Summarised from Revolution Medicines's posting. Read the full original.
Listed by Revolution Medicines on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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