Regulatory Data Steward & Team Lead

About the role

The Regulatory Data Steward & Team Lead is responsible for creating and maintaining master data within Pfizer’s Veeva Vault RIM system. This senior position ensures that all regulatory metadata is accurate, complete, and compliant with health authority requirements, supporting global regulatory submissions and product safety.

Key responsibilities

• Lead the definition, creation, and maintenance of core/master data, including IDMP identification of medicinal products.
• Oversee application and registration creation, deciding when to create new objects or use existing ones.
• Verify and update data in Veeva Vault RIM, execute approved change requests, and resolve data quality issues.
• Collaborate with Regulatory Strategy, CMC leads, Clinical, Non‑Clinical, RIO, labeling groups, and enterprise‑wide data governance teams.
• Support strategic initiatives by providing insights on data standards and digital transformation within Global Regulatory Sciences.

Required profile

• Significant experience with regulatory data and master data management in a pharmaceutical environment.
• Strong understanding of Veeva Vault RIM, IDMP standards, and data governance policies.
• Proven ability to work with cross‑functional teams and drive data quality improvements.
• Senior‑level expertise, capable of influencing strategy and execution.

Required skills

• Veeva Vault RIM
• IDMP (Identification of Medicinal Products)
• Master Data Management
• Regulatory data systems
• Data governance

What we offer

• Opportunities for growth in operations, strategy, and digital domains.
• Exposure to global regulatory processes and cutting‑edge digital tools.