US Medical Director for Rare Hemophilia

About the Opportunity:

This is an exciting opportunity to join Pfizer's US Medical Affairs team as a Senior Medical Director for Rare Hemophilia. As a member of this team, you will play a critical role in shaping the medical strategy for rare hemophilia, working closely with cross-functional teams to develop and execute medical affairs operating plans, and providing medical leadership and strategic direction to support successful product development and commercialization.

Key Responsibilities:

• Develop and Execute Medical Affairs Operating Plan: Develop and execute the rare hemophilia medical affairs operating plan, ensuring alignment with global medical strategies and objectives.
• Provide Medical Leadership: Provide medical leadership and strategic direction to cross-functional teams, including clinical and commercial development plans, to ensure successful product launch and commercialization.
• Establish Critical External Relationships: Establish and maintain critical external relationships with US thought leaders and professional societies in the hemophilia therapeutic area, ensuring collaboration and alignment on key initiatives.
• Represent US Medical Affairs: Represent US Medical Affairs on hemophilia-related cross-functional teams, ensuring effective communication and coordination across functions.
• Develop and Execute US Medical Strategies: Develop and execute US medical strategies for phase IV research, including real-world evidence (RWE) and data generation plans, to support business objectives.
• Lead Data Generation and Analysis: Lead data generation and analysis efforts, ensuring the accuracy and scientific integrity of manuscripts, abstracts, and posters.
• Partner with Field Medical Leadership: Partner with Hemophilia Field Medical leadership to integrate insights into strategy development and execution, ensuring seamless and coordinated partnership.
• Manage Budget and Resources: Ensure timely and appropriate management of the US Hemophilia Medical budget, including project spend and resource allocation.
• Provide Medical Input: Provide medical input on US labeling and regulatory interactions, ensuring compliance with regulatory requirements.
• Lead Advisory Boards and Congress Planning: Lead and execute successful Medical advisory boards and congress-related symposia, ensuring high-quality content and outcomes.
• Participate in Medical Subcommittee: Participate in the Medical Subcommittee (MSC), consisting of cross-functional medical colleagues, including outcomes research, to drive medical excellence and innovation.
• Develop HCP Engagement Plans: Develop and maintain HCP engagement plans for HQ Medical Affairs, ensuring effective communication and relationship-building.
• Provide Commercial Leadership: Provide medical leadership in US Commercial initiatives, supporting brand positioning, promotional materials, and digital projects.
• Serve as Voice of US Medical: Serve as the voice of US Medical, ensuring US Hemophilia needs are considered and represented in Global Medical strategies.
• Collaborate with External Partners: Collaborate with US external partners to further scientific insights and data generation, driving business impact and growth.
• Mentor and Coach Colleagues: Mentor and coach other colleagues, as appropriate, to foster a culture of excellence and continuous learning.
• Build Trust and Credibility: Build trust among team members and broader stakeholders by setting a highly visible example of medical integrity and excellence.