Director, Regulatory Operations, Systems

Revolution Medicines•Redwood City, CA

2d•Hybrid

About The Position

Revolution Medicines is a global, commercial-stage oncology company dedicated to discovering, developing, and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide. Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency, and hold ourselves to a high standard of rigor—all in service of patients. The Opportunity: The Director Regulatory Operations will partner closely with the Senior Director and Head of Regulatory Operations and Planning to build, lead, and scale Revolution Medicines’ regulatory information management capabilities. This role will set the strategy, oversee implementation, and manage optimization of the company’s global regulatory systems and processes, with a primary focus on the Veeva Vault RIM platform and associated technologies. This is a build-and-scale role. The Director will provide hands-on leadership in establishing processes, optimizing systems, and ensuring operational excellence, while also shaping the long-term vision and future capabilities of the RIM function. The role includes preparing the organization for future structured data submission requirements — such as Veeva Registrations, IDMP readiness, and eCTD 4.0 — and collaborating across Regulatory Affairs, Clinical Development, Quality, Information Sciences (IS), IT, and other functions to establish integrated global processes. The Director will also identify opportunities to introduce innovative solutions — such as automation or AI — where appropriate to improve efficiency and data quality.

Requirements

Bachelor’s degree in a life science, technical, or related field with 12+ years of experience in the biotechnology, pharmaceutical, or medical device industry, with at least 3–5 years focused on Regulatory Affairs/Operations and Veeva RIM systems (administration, configuration, and optimization).
Experience submission management in EU, Japan, and Canada.
Proven leadership experience, including building functions, managing small teams, and leading cross-functional initiatives.
Strong understanding of global regulatory submission requirements and evolving Health Authority standards.
Expertise in eCTD specifications, electronic submissions, and regulatory publishing standards.
Experience with system implementation, validation, and compliance under GxP regulations.
Excellent communication, stakeholder engagement, and change management skills, with the ability to influence and drive adoption across diverse teams.
Bachelor’s degree in Life Sciences, Engineering, Information Systems, or related field (advanced degree preferred).

Nice To Haves

Advanced knowledge of Veeva Vault RIM and related regulatory systems.
Experience supporting oncology drug development and regulatory submissions across the full product lifecycle (IND through post-marketing).
Familiarity with structured data submissions, including Veeva Registrations, IDMP readiness, and eCTD 4.0 standards.
Prior experience in digital transformation initiatives, including system integrations and process automation.
International experience with global submissions and regional regulatory requirements.
Understanding of IT system architecture, cloud solutions, and integrations in a GxP-regulated environment.

Responsibilities

Partner with the Head of Regulatory Operations to establish and lead the Regulatory Information Management function, including governance, process ownership, and roadmap development.
Define and execute the long-term RIM strategy to align regulatory systems and processes with business objectives and global compliance standards.
Build the foundation for the RIM function by balancing strategic planning with hands-on leadership to establish processes, optimize systems, and drive operational excellence.
Partner with stakeholders to prioritize initiatives, drive digital transformation, and ensure readiness for future regulatory data submission requirements.
Position the RIM function as a strategic contributor by improving visibility, streamlining processes, and delivering business value through accurate, compliant regulatory data.
Represent Regulatory Operations in planning discussions and enterprise initiatives, collaborating closely with cross-functional teams to deliver integrated solutions.
Serve as the business owner for the Veeva Vault RIM platform, overseeing administration, configuration, data integrity, and ongoing enhancements.
Manage system implementation, upgrades, validation, and change management activities.
Collaborate with IT, Veeva, and vendors to integrate RIM with other enterprise systems (e.g., eTMF, CTMS, QMS) and ensure seamless workflows.
Lead RIM release management, communicate system updates, and develop training plans to ensure optimal adoption.
Oversee RIM data quality, including monitoring, governance, master data management, and compliance remediation.
Establish metadata standards and implement processes to ensure consistent data stewardship across all regulatory systems.
Drive continuous improvement of regulatory submission processes and tools to support global Health Authority interactions and international filing requirements.
Provide strategic input into submission planning, timelines, and resource allocation.
Partner with the Global Regulatory Affairs department to streamline workflows, reduce manual effort, and improve submission quality.
Develop and maintain SOPs, work instructions, and job aids related to regulatory systems and submissions.
Ensure processes and systems are designed to meet structured data submission requirements (e.g., Veeva Registrations, IDMP, eCTD 4.0).
Partner with stakeholders across Regulatory, Clinical, Quality, IS, IT, and external vendors to align processes, resolve issues, and implement best practices.
Serve as the primary liaison between Regulatory Affairs and system vendors to ensure compliance and functionality meet evolving business needs.
Engage proactively with business partners to demonstrate the value of regulatory data and systems, positioning the RIM function as a key enabler rather than a back-office resource.
Provide expertise to support inspections, audits, and regulatory authority interactions related to RIM systems and data.
Build, mentor, and manage a high-performing team responsible for regulatory systems and data management.
Potentially hire and manage a Data Steward and Archivist to support regulatory data integrity and compliant archival practices, contingent upon budget approval and business needs.
Currently manage one direct report, with potential to expand the team as the function evolves.
Develop and deliver training programs to improve system utilization and regulatory compliance.
Promote a culture of innovation, operational excellence, and continuous improvement within Regulatory Affairs.
Evaluate and recommend innovative solutions — such as automation or AI — where appropriate to improve regulatory data management, submissions, and reporting.
Stay current with evolving regulatory technology trends and propose enhancements that deliver measurable business value.