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Director, US Public Policy

Merck

Washington, DCHybridPosted 1 day ago$190,800.00 - $300,300.00
Full TimeDirector & AboveRegulatory AffairsPharmaceutical
Original posting ↗

Summary

Our company's Global Policy and Public Affairs (GPP) organization works with policymakers, public health leaders, patient and provider organizations, trade associations, coalitions, and other stakeholders to advance public policies that support innovation and improve patient access to medicines and vaccines. The U.S. Federal Policy and Government Relations team within GPP is seeking a public policy leader with a law degree and experience in public health matters to serve as Director, U.S. Public Policy.

Job description

The Director will lead policy development and execution for vaccines and for our company's investigational long-acting influenza antiviral (a non-vaccine approach to influenza) and provide legal and policy analysis across the broader public policy portfolio, including access, oversight, intellectual property, research and development, etc. The successful candidate will combine broad public policy knowledge, public health experience, and strong legal analysis and drafting skills to develop practical recommendations and build alignment across a highly matrixed organization, including colleagues in medical, commercial, legal and other subject-matter experts.

Primary Responsibilities

  • Lead policy development and execution for vaccines and for our company's investigational long-acting influenza antiviral; monitor and assess related federal, regulatory, and administrative developments across public health, prevention, access, coverage, reimbursement, and health-system infrastructure.
  • Work with the team to support legal analysis of issues across the public policy portfolio, in coordination with the issue lead and legal counsel, as needed, including pricing, reimbursement, access, intellectual property, and oversight.
  • Develop evidence-based company policy positions, comment letters, and other policy submissions, integrating public health evidence, legal analysis, and business considerations in partnership with cross-functional colleagues.
  • Translate complex policy developments into clear insights, implications, options, and recommendations for senior policy and business leaders.
  • Identify emerging risks and opportunities and develop proactive strategies to advance or protect priority policy outcomes.
  • Build and maintain relationships with government officials, public health organizations, patient and provider groups, policy organizations, and other partners, and represent our company in trade association and coalition meetings.
  • Lead cross-functional policy workstreams from strategy through execution, including workplans, decision points, stakeholder roles, budgets, and measures of progress or impact.
  • Manage policy research, consultants, and other resources that strengthen policy development, thought leadership, and advocacy strategies.

Required Qualifications

  • Juris Doctor (J.D.) or equivalent law degree required.
  • At least seven years of relevant experience in public policy, government, public affairs, a trade association, a patient or provider organization, consulting, or the biopharmaceutical sector.
  • Demonstrated knowledge of U.S. public policy and the legislative, regulatory, and administrative policymaking processes at the federal and/or state level.
  • Experience addressing public health matters and the ability to lead policy work on vaccines and on a long-acting antiviral influenza product while contributing to broader public policy issues, including pricing, reimbursement, and patient access.
  • Sound judgment and strong legal research, analysis, and drafting skills, with the ability to work through unfamiliar issues, develop practical recommendations, and collaborate effectively with legal counsel and subject-matter experts.
  • Excellent written and verbal communication skills, including the ability to communicate effectively with senior leaders and high-level external stakeholders.
  • Demonstrated experience working across culturally teams and matrixed teams with a high degree of collaboration.

Required Skills

Healthcare Policies, Patient Advocacy, Policy Analysis, Policy Development, Political Forums, Public Health, Public Policies, Regulatory Development, Strategic Planning, Strategic Thinking

Requirements

  • Juris Doctor (J.D.) or equivalent law degree required
  • At least seven years of relevant experience in public policy, government, public affairs, a trade association, a patient or provider organization, consulting, or the biopharmaceutical sector
  • Demonstrated knowledge of U.S. public policy and the legislative, regulatory, and administrative policymaking processes at the federal and/or state level
  • Experience addressing public health matters and leading policy work on vaccines and long-acting antiviral influenza products
  • Ability to contribute to broader public policy issues including pricing, reimbursement, and patient access
  • Sound judgment and strong legal research, analysis, and drafting skills
  • Ability to work through unfamiliar issues and develop practical recommendations
  • Ability to collaborate effectively with legal counsel and subject-matter experts
  • Excellent written and verbal communication skills
  • Ability to communicate effectively with senior leaders and high-level external stakeholders
  • Demonstrated experience working across culturally diverse and matrixed teams with a high degree of collaboration
  • Healthcare Policies
  • Patient Advocacy
  • Policy Analysis
  • Policy Development
  • Political Forums
  • Public Health
  • Public Policies
  • Regulatory Development
  • Strategic Planning
  • Strategic Thinking

Benefits

  • Medical, Dental & Vision
  • Retirement Benefits
  • 401(k)
  • Paid Holidays
  • Vacation
  • Compassionate Leave
  • Sick Days
  • Annual Bonus
  • Long-Term Incentive

Company overview

Merck & Co., Inc., known as Merck in the United States and Canada and MSD (Merck Sharp & Dohme) internationally, is a premier American multinational pharmaceutical company headquartered in Rahway, New Jersey. Founded in 1891 as the U.S. subsidiary of the German Merck Group, the company became independent following World War I and has since grown into one of the world's largest biomedical companies, ranking fourth globally by revenue. Merck operates across three core business segments: pharmaceuticals, vaccines, and animal health products. The company is renowned for its groundbreaking research and development, having brought numerous life-saving medicines to market including Keytruda (pembrolizumab), a leading immunotherapy for cancer treatment that generated $29.5 billion in 2024 revenue, and Gardasil, a revolutionary HPV vaccine. With approximately 75,000 employees worldwide, Merck maintains a robust pipeline of innovative therapies focused on oncology, vaccines, hospital acute care, cardiology, neuroscience, virology, immunology, and diabetes. The company invests heavily in R&D, spending $17.9 billion in 2024 alone, demonstrating its commitment to advancing scientific discovery. Merck's legacy spans over 130 years of bringing hope to humanity through important medicines and vaccines, operating with a purpose to use leading-edge science to save and improve lives globally while fostering an inclusive workforce and responsible business practices.

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