Director, Regulatory Information Management (Onsite Hybrid)

Company Description

AbbVie'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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

The Director of Regulatory Information Management (RIM) leads the advancement of business capabilities to enable efficient, consistent, and compliant use, and management, of Regulatory information across AbbVie and with Health Authorities. Provides strategic design, implementation, and ongoing improvements of Regulatory business capabilities. Works closely with Business Process Owners across the enterprise to identify, prioritize, and deliver integrated processes involving Regulatory Information and supporting technologies in support of our broader AbbVie strategies. In addition, the individual has division level influence and is generally considered a key opinion leader and an expert resource both within AbbVie and externally. The individual may influence changing regulations and guidance, interface with outside regulatory agencies and provide executive management with RIM metrics and reports.

Additional Responsibilities Include: 

• Proposes and executes enhancement within the Regulatory Information management vision. Provides strategic design, development, and implementation plans for the RIM Solution (Cosmos), and works alongside BTS, Business SMEs, and stakeholders to propose and lead the execution of these plans.
• Will partner across multiple functions to influence and provide leadership on new opportunities for enhanced digital and information management capabilities working to drive digital change. This leader will collaborate across the enterprise with leaders from Data Science, Clinical, Safety, Manufacturing, Quality, and Commercial to identify opportunities to improve outcomes, operational efficiencies, and quality across the E2E regulatory lifecycle.
• The leader partners with IT on identifyi