PMA Companies

Compliance

• Support domestic and international regulatory policy and advocacy efforts
• Drive development, evaluation, and execution of advocacy priorities in collaboration with SRA colleagues
• Develop and execute projects related to science and regulatory advocacy
• Coordinate Work Groups to ensure alignment with PhRMA policy positions
• Serve as a point of contact for internal and external stakeholders on select topics
• Develop and present project proposals to leadership
• Maintain relationships with external stakeholders like regulatory bodies and industry associations
• Perform other duties as assigned

Director, Science and Regulatory Advocacy

• Provide leadership and strategic development for regulatory policy and advocacy efforts
• Lead and manage the execution of projects related to science and regulatory advocacy
• Build and maintain relationships with key external stakeholders
• Represent industry/PhRMA externally to third parties
• Perform other duties as assigned

Deputy Vice President, Science and Regulatory Advocacy

Director

• Develop and maintain relationships with Congress members
• Lobby Senate Democratic members on potential legislation
• Coordinate policy positions and legislative strategies
• Build and maintain relationships with stakeholders
• Represent Federal Advocacy team in internal meetings
• Analyze legislation relevant to industry priorities
• Manage consultants for the Federal Advocacy team
• Perform other duties as assigned

Senior Director, Federal Advocacy

• Lobby lawmakers on the Ways and Means Committee, House Republican members and their staff on potential/proposed legislation and the impact of such legislation on patients and the pharmaceutical industry
• Coordinate with PhRMA colleagues and member company staff on policy positions and the development of legislative strategy related to PhRMA priorities
• Anticipate, track and analyze legislation relevant to industry priorities, involving PhRMA staff and member company representatives as needed
• Represent the Federal Advocacy team at internal PhRMA meetings and collaborate across departments on policy, engagement strategy and messaging materials
• Build and maintain relationships with Member company staff and other stakeholders
• Manage consultants who provide services to the Federal Advocacy team
• Perform other duties as assigned

Director, Federal Advocacy

Manager

• Develop subject matter expertise on the 340B program and issues related to hospital pricing
• Keep current on trends, research studies and third-party policy analyses related to 340B and hospital finances
• Work closely with colleagues in other departments to support education and advocacy initiatives on 340B
• Develop slides, talking points and other materials across a range of issues related to 340B
• Oversee and coordinate research projects being managed by outside consultants
• Support work to analyze regulations and draft comment letters
• Provide technical expertise and develop materials to support State advocacy efforts
• Assist with member workgroup calls and coordinate the development of materials related to those calls

Director, Science and Regulatory Advocacy

Deputy Vice President, Science and Regulatory Advocacy

Senior Director, Federal Advocacy

Director, Federal Advocacy

Senior Manager, Policy & Research – Federal Programs