Director, Regulatory Information Management

Revolution Medicines; San Francisco (CA); On-site; USD 211,000 - 264,000; Full time

Benefits offered by this job

Robust equity awards

Strong benefits

Learning and development opportunities

Job summary

Revolution Medicines is seeking a Director of Regulatory Operations to lead and scale its regulatory information management capabilities. The role focuses on the Veeva Vault RIM platform, governance, and end-to-end data quality across global submissions.

You will collaborate across Regulatory Affairs, Clinical Development, Quality, Information Sciences, and IT to implement scalable processes and innovative solutions.

Qualifications

• Bachelor's degree in life science, technical, or related field; 12+ years in biotech/pharma with 3–5 years in Regulatory Affairs/Operations and Veeva RIM
• Experience with EU, Japan, and Canada submissions; knowledge of eCTD and regulatory publishing standards
• Proven leadership, ability to build and manage cross-functional programs, and drive regulatory data integrity

Responsibilities

• Lead Regulatory Information Management with governance, ownership, and roadmap development.
• Define long-term RIM strategy aligning regulatory systems with business goals and global compliance.
• Establish processes and optimize RIM systems (Veeva Vault RIM) and ensure readiness for future data submissions.
• Drive continuous improvement of submission workflows for global Health Authority interactions.
• Collaborate with Regulatory, Clinical, Quality, IS, IT, and vendors to implement best practices.
• Build and mentor a high-performing team and develop training on regulatory data management.

Skills

Regulatory leadership

Regulatory submissions

Global regulatory standards

Cross-functional collaboration

Education

Bachelor's degree in Life Sciences / related field

Tools

Veeva Vault RIM

Job description

Revolution Medicines is seeking a Director of Regulatory Operations to lead and scale its regulatory information management capabilities. The role focuses on the Veeva Vault RIM platform, governance, and end-to-end data quality across global submissions.

You will collaborate across Regulatory Affairs, Clinical Development, Quality, Information Sciences, and IT to implement scalable processes and innovative solutions.