Director, U.S. Public Policy (FDA)

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, U.S. Policy will monitor, track, and analyze key U.S. Food and Drug Administration (FDA) public policy issues that could impact AbbVie and the patients we serve. The Director will be the lead within the U.S. Policy & Analytics (USPA) team for all legislative and regulatory policy developments related to FDA. The Director will work with internal stakeholders to determine the impact of new policies, develop policy positions, and work with the Federal Government Affairs (FGA), State Government Affairs (SGA), U.S. Strategic Alliances, Regulatory Affairs (RA), Corporate Affairs and Legal teams to develop advocacy strategies. The Director will also identify emerging policy trends of interest to AbbVie and develop recommendations on how to prepare for threats and opportunities. The Director will be responsible for communicating changes in policies, trends, and/or other significant developments at the federal level to key internal stakeholders.  The Director will also support the FGA, SGA, RA, U.S. Strategic Alliances, and Legal teams in developing advocacy materials and messages that clearly articulate AbbVie’s position and/or strong counter arguments. The Director will be the strategic partner to senior leaders in the organization leading FGA, SGA, RA, USPA, Global Policy & U.S. Access Strategies (GPAAS), Corporate Affairs, and Legal. The Director will set the federal policy priorities and strategically engage partners to generate enterprise-wide support and resources necessary to accomplish our goals.

Core Responsibilities

• Identify, track, and analyze FDA legislative and regulatory developments that impact AbbVie and its products.
• Work with