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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 XFacebookInstagramYouTubeLinkedIn 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 internal stakeholders to determine how federal legislative and regulatory developments related to FDA reform impact AbbVie and the patients we serve.
  • Develop clear and effective communications to ensure that internal AbbVie stakeholders are aware of and understand key issues and developments.
  • Provide internal expertise on federal policy and develop policy materials such as talking points, policy papers, and legislative/amendment language, in collaboration with legal, to support FGA, RA, U.S. Strategic Alliances and Legal colleagues in driving adoption of AbbVie priorities and policy positions.
  • Develop novel policy ideas/options in collaboration with internal AbbVie stakeholders and ensure that positions are aligned with key business objectives, in collaboration with the key partners.
  • Create persuasive materials and compelling messages for the FGA and GPAAS team to utilize in their communications with policymakers and third-party stakeholders.
  • Work closely with the GA Therapeutic Area Strategies team and above brand internal colleagues to understand brand strategies and incorporate key insights into policy analyses and development.
  • Develop, direct, and manage external analysis, projects, and other initiatives supported by external consultants.
  • Ensure alignment with International Policy functions to ensure global consistency of AbbVie’s public policy positions.
  • Represent AbbVie in external policy discussions, as needed, to position AbbVie as an industry thought leader.
  • Lead discussion with senior leaders at AbbVie to garner cross functional support for our initiatives including leaders in FGA, RA, GPAAS, Corporate Affairs, and Legal.

Qualifications

 

  • Minimum ten years of experience in progressively more responsible roles.
  • Must possess significant experience and deep technical expertise in FDA legislative and regulatory policy.
  • Relevant experience in health care with a focus on pharmaceuticals policy required, as well as an understanding of the role of government agencies in health policy at the federal level, and an understanding of the interaction between international, federal and state issues.
  • Ability to identify policy opportunities and challenges, to connect policy to commercial business impact, and to develop concise and persuasive public policy positions and other written materials within the context of the political environment.
  • Exceptional communicator (verbal, written, presentations). Ability to effectively communicate public policy information and positions to internal and external stakeholders.
  • Must be able to work collaboratively with multiple cross-functional peers, handle ambiguity well, and enjoy working in a collegial, yet fast-paced and high performing environment.
  • Strong analytical, critical thinking, and organizational skills; strong attention to detail.
  • Bachelor's degree in related field such as public policy, health care administration, or political science required. Advance degree preferred (MPH, MBA, JD, MPP, PhD).
  • Some domestic travel (15 percent) required.

Key Stakeholders

Internally – Federal Government Affairs, State Government Affairs, Regulatory Affairs, U.S. Policy & Analytics, Global Policy & U.S. Access Strategies, Corporate Affairs, and Legal. Externally – consultants, third party groups, and peer companies.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

  • This job is eligible to participate in our short-term incentive programs. ​

  • This job is eligible to participate in our long-term incentive programs​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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CEO of AbbVie
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Richard A. Gonzalez
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Average salary estimate

$190000 / YEARLY (est.)
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$150000K
$230000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

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AbbVie’s mission is to discover and deliver innovative medicines 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: i...

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Full-time, onsite
DATE POSTED
October 20, 2025
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