Compliance

• The Regulatory Data Steward is accountable for the creation and maintenance of V-RIM Master Data on behalf of the organization
• Responsible & accountable for the creation & maintenance of core/master data inclusive of identification of Medicinal Products (IDMP) and creation of applications
• Work in close collaboration with Regulatory Strategy, CMC Leads, Clinical, Non-Clinical, RIO and labelling groups to generate and maintain data
• Form a partnership with Data Coordinators and RIDGE/enterprise-wide Data Governance teams
• Support strategy implementation, bridging strategy and execution, providing crucial insights and feedback at the strategic level
• A percentage of the role will be dedicated to harnessing Veeva data and to advance the digital landscape within Global Regulatory Sciences

Regulatory Data Steward, Manager

Regulatory Data Steward – Team Lead