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Principal Capability Professional for Registration Tracking xEVMPD

Sanofi
Remote friendly (Cambridge, MA)
United States
Operations

Role Summary

Principal Capability Professional for Registration Tracking xEVMPD leads strategic transformation and innovation of Registration Tracking, Data Information Flow & Transactions Capability, driving compliance excellence, user experience, and process consistency. Defines and drives cross-domain capability roadmaps with enterprise impact, serving as a strategic bridge between regulatory SMEs, business process owners, and digital product teams to develop scalable, compliant solutions that support regulatory strategy.

Responsibilities

  • Define and drive cross-domain capability roadmaps with enterprise impact.
  • Contribute to enterprise-level process architecture and governance, balancing standardization and innovation.
  • Design and orchestrate complex workshop programs and testing strategies to support solution development and validation.
  • Develop enterprise compliance strategies and risk mitigation approaches.
  • Represent the organization during critical audits and regulatory inspections related to Registration Tracking and Data Information Flow Capability.
  • Drive transformational process improvements with significant ROI across end-to-end regulatory capabilities.
  • Serve as Business System Owner (BSO) for Veeva RIM, overseeing governance, documentation, and strategic alignment.
  • Manage Registration Tracking backlog in JIRA and triage against Back to Standard Program.
  • Lead resolution of Level 3 support issues and complex modeling challenges.
  • Evaluate and champion strategic technology investments in regulatory capability development, digital adoption, and AI.
  • Analyze Veeva releases and roadmap critical features for future adoption.
  • Contribute to structured data submission readiness (gradual IDMP implementation in multiple regions, such as PMS enrichment for Europe).
  • Design enterprise change management frameworks and governance with Training and Communication teams.
  • Facilitate Functional Lead forums and present best practices to Super Users.
  • Develop talent and lead workstreams across Regulatory, Digital, and Data Governance.
  • Focus on end-to-end flow of regulatory registration tracking data across stages, departments, and systems; manage Events, Activities, Regulatory Objectives, Workflows, Wizards, Impact Assessments, and Health Authority Interactions.
  • Collaborate with Process Owner (GRO) and Product Owner (Digital) for alignment between system development and process operationalization.
  • Lead cross-functional initiatives to enable effective Capability delivery.

Qualifications

  • Experience: 10+ years with demonstrated leadership in regulatory operations.
  • Soft Skills: Expert communication and collaboration within a matrixed organization; proven ability to lead, influence, and drive change in a fast-paced, cross-functional environment.
  • Technical Skills: Expert knowledge of Veeva Vault RIM Registration Tracking, IDMP standards, and structured data submissions; recognized authority in business process optimization in regulatory affairs; expert understanding of capability-based planning, agile delivery, and digital product lifecycles; strategic vision for digital tools, automation, and AI implementation.
  • Languages: Fluent in English (spoken and written).

Skills

  • Business process optimization in regulatory affairs
  • Capability-based planning and agile delivery
  • Digital product lifecycles and AI implementation
  • Veeva Vault RIM Registration Tracking and IDMP standards
  • Regulatory data governance and submission readiness

Education

  • BS/BA required
  • Master's degree or specialized training preferred

Certifications

  • Advanced certifications in LEAN, Agile, BPM or equivalent preferred

Additional Requirements

  • None specified beyond job-related qualifications.