Coordinates release readiness and lifecycle management for 60+ Veeva RIM integrations. Tracks dependencies, risks, remediation, testing, validation, stakeholder communications, cutover activities, and operational handoffs. Partners with product, regulatory, technical, quality, vendor, and consuming application teams to assess Veeva RIM data model impacts and ensure integration changes meet Agile, SDLC, and CSV expectations.

Supports global and regional pharmaceutical regulatory strategy, lifecycle maintenance submissions, CMC Module 1 preparation, labeling updates, safety reporting, and Health Authority responses. Coordinates submission components, performs quality checks, maintains regulatory trackers, and collaborates with global, regional, country, clinical, safety, quality, supply, and commercial teams. Contributes to process improvement, automation, and standardized regulatory workflows while ensuring timely, accurate, and compliant deliverables.