Director, Regulatory Affairs Data Standards and Governance

Director, Regulatory Affairs Data Standards and Governance

• Full‑time
• Salary Min: 160500
• Salary Max: 305000
• Workday Global Grade: 21
• Compensation: USD 160,500 - USD 305,000 - yearly

Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience— and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at  Follow @abbvie on Linked In, Facebook, Instagram, X and You Tube.

The Director, Regulatory Affairs Data Standards and Governance is responsible for driving awareness and implementation of data standards and associated best practices in systems to support Regulatory Requirements for data submissions and to enable Regulatory data to connect with data sourced from other functions including R&D Development, Supply Chain, Operations and Quality Assurance. This role has functional responsibilities within RIM, in addition to performing a key role within the cross‑functional Enterprise Product Master Data (EPMD) Data Office initiative.

• Demonstrates leadership within the Product Data Governance Office, building and executing lean and effective Data Governance processes.
• Support the Product Data Office initiative to establish enterprise‑level data governance, improve data quality and interoperability to resolve key business challenges including Regulatory and Supply Chain data integration and Change Control processes.
• Through Data Office engagement, works with cross‑functional colleagues to define and implement consistent processes for data standards implementation across Abb Vie. Accomplished by building detailed knowledge of external standards applicable to Regulatory business processes and submissions including:
  • EMA standards (published through the SPOR platform)
  • FDA Data Standards Catalogue
  • World Health Organization (WHO) for ATC Codes and INN
  • International Conference on Harmonization (ICH)
• Builds and uses Abb Vie’s Data Catalogue to drive clear definitions for critical data elements, supporting data lineage verification and mapping properties across systems for interoperability of Regulatory data across the product lifecycle.
• Demonstrates detailed knowledge of ISO IDMP requirements, and how the ISO IDMP standard is being implemented by Health Authorities globally. As an IDMP SME, advocate for Abb Vie’s interest in industry forums and collaborates with RPI colleagues to share knowledge learned through industry engagement and assess the impact to Abb Vie’s Regulatory systems and processes.
• Ensure that Abb Vie’s interests are represented in external industry forums for cloud‑based submissions, structured data submissions, eCTD4, structured content authoring and the implementation of Regulatory industry standards. Prepare Abb Vie for the implementation of regulatory requirements on data submission topics to ensure sustained compliance with Health Authority requirements.
• Collaborates with EKS (Enterprise Knowledge Services) to build Abb Vie’s central Ontology services for Regulatory and Enterprise use, incorporating external standards published by organizations including ISO, WHO, ICH and Health Authorities.
• Supports the rollout, implementation and training of analysis tools which aid comparison of Abb Vie system dictionary terms and data to enterprise standards maintained in the Ontology to support cross‑system and cross‑functional data harmonisation, remediation and synonym matching.
• Engages with and communicates on data enrichment and harmonisation projects linked to system interoperability projects thus driving overall awareness.
• Support consistent data entry within COSMOS RIM by monitoring and maintaining system dictionaries and vocabularies in alignment with enterprise standards to support data submissions, FHIR projects and, to prepare Abb Vie to meet Regulatory compliance e.g. EU IDMP.
• Work with RIM colleagues to deliver COSMOS system releases that drive further automation,…