Director, U.S. Therapeutic Area Strategies (Oncology/Specialty)

The Director of U.S. Therapeutic Area Strategies (TAS) is responsible for devising and implementing comprehensive government affairs strategies that drive therapeutic area specific policy initiatives to remove barriers to access and promote above brand policy solutions that support AbbVie’s business objectives.  The position will serve as the liaison between the U.S. Government Affairs and the U.S. Oncology and Specialty Business Units sharing business developments, risks and opportunities with U.S. Government Affairs colleagues and providing legislative intelligence and insights to the brand teams.  In this capacity, the Director of U.S. TAS will 1) identify opportunities to advance Government Affairs strategies to support TA or above brand objectives, 2) ensure GA colleagues are aware of critical business drivers, challenges and developments related to the oncology and specialty portfolios in the U.S., 3) build and sustain advocacy partnerships that help advance our therapeutic areas policy solutions, and 4) collaborate with GA partners to provide relevant policy related insights or advocacy updates with the U.S. Oncology and Specialty Business Units.

Responsibilities:

•Support the Oncology and Specialty Business Units in creating a more favorable public policy environment for AbbVie’s business activities by shaping government policies in order to positively affect patient access and reimbursement among government and commercial players for oncology brands in the U.S.

•Serve as a resource and connector for U.S. Government Affairs function to the Oncology and Specialty Business Units by ensuring close alignment and understanding of commercial and pipeline priorities with public policy goals and focus on advancing access opportunities and addressing access challenges in the U.S.

•Establish, develop and maintain relationships with third party organizations.  Drive aligned policy advocacy strategies with third party organizations and seek to achieve productive long-term working relationships with partners.  Undertake regular and rigorous product/therapeutic area-oriented assessment of government affairs and policy environment to develop, review and update engagement plans with external stakeholders. 

•Serve as the Government Affairs designated partner for the US brand teams in oncology and specialty.  Support and align with brand teams for brand planning, strategy development and capacity building across a product’s life cycle.  Mobilize appropriate policy, public affairs and government affairs resources to ensure implementation of comprehensive government affairs strategies. 

• Develop and drive GA launch readiness approach in collaboration with U.S. Government Affairs and other core functions. Align with U.S. Federal and State Government Affairs teams and Global Policy and Alliance Access Strategies team to provide on-going advice and guidance to the Oncology and Specialty Business Units on policy and political developments that directly impact oncology and specialty brands or above brand issues.  Anticipate trends in external environment that will impact oncology and specialty and develop plans to address areas of concern.   Provide strategic counsel to U.S. brand teams while also ensuring alignment with corporate policy positions.

•Collaborate cross-functionally with internal stakeholders to ensure global alignment of strategies.  Align with Global TAS team members to inform and support early brand strategy development and engagement efforts for pipeline products.

• Manage consultants and budget to effectively resource public policy advocacy strategies. 

Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required