Senior Director, RIM Strategy & Global Submissions

Revolution Medicines, Inc.; San Francisco (CA); On-site; USD 244,000 - 305,000; Full time

Job summary

Revolution Medicines, Inc. is seeking a Senior Director of Regulatory Information Management (RIM) to build and scale global regulatory systems, led by Veeva Vault RIM. The role shapes strategy, governance, and data quality across Regulatory Affairs, Clinical Development, Quality and IS.

Based in Redwood City, CA, this onsite position emphasizes process optimization, regulatory submissions readiness (IDMP, eCTD 4.0) and opportunities for automation and AI to drive efficiency.

Qualifications

• 14+ years in biotech/pharma/medical device with 7+ years in Regulatory Affairs/Operations and Veeva RIM
• Experience with EU, Japan, and Canada submissions
• Proven leadership building functions and leading cross-functional initiatives
• Excellent communication, stakeholder engagement and change management skills
• Experience with IT system architecture, cloud solutions, and GxP compliance

Responsibilities

• Lead Regulatory Information Management function, governance and roadmap
• Define long-term RIM strategy aligned with global compliance
• Oversee data quality, master data management and metadata standards
• Collaborate with IT, Veeva, and vendors for system integrations
• Prepare for structured data submissions (Veeva Registrations, IDMP, eCTD 4.0)
• Partner with stakeholders to drive digital transformation and readiness

Skills

Veeva Vault RIM

Regulatory Affairs/Operations

Leadership

Stakeholder engagement

Change management

Communication

Education

Bachelor's degree in Life Sciences, Engineering, Information Systems, or related field

Advanced degree preferred

Tools

Veeva Vault RIM

eCTD 4.0

IDMP readiness

Regulatory submissions systems

Job description

Revolution Medicines, Inc. is seeking a Senior Director of Regulatory Information Management (RIM) to build and scale global regulatory systems, led by Veeva Vault RIM. The role shapes strategy, governance, and data quality across Regulatory Affairs, Clinical Development, Quality and IS.

Based in Redwood City, CA, this onsite position emphasizes process optimization, regulatory submissions readiness (IDMP, eCTD 4.0) and opportunities for automation and AI to drive efficiency.