Director, Patient Advocacy
2 weeks ago
ROLE SUMMARY
The Platform functions to:
enhance Pfizer’s ability to determine unmet medical needs; support differentiated product labels for Product Development programs including finding alternatives and accelerated licensure pathways for new indications through the use of Real World Data (RWD), Real World Insights (RWI) and RWE; inform clinical practice on appropriate prescription and use of Pfizer’s products; in collaboration with Access & Value, strengthen the value evidence package for payers and access/policy decision-makers; support measurement of short
- and long-term impact of Pfizer’s products to both patients and populations; support competitive differentiation.
The opportunity: Reporting to the Head of Patient Advocacy & External Partnerships, this role is critical for the RWE Platform to ensure that the voice of the patient is at the center of our work. They will coordinate closely with RWE Strategic Planning & Business Operations Leaders, as well as those from other RWE teams and cross-functional partners as assigned, to execute on a vision for inclusion of patients / patient advocates in key strategic tactics as part of a comprehensive integrated evidence plans & RWE generation priorities. Any operating model must take into account the need to scale over time and the inclusion of voices from different countries and regions. They will also seek to engage with patients and patient advocacy groups to garner their support for evidence interpretation and dissemination, giving their voice and positions to the appropriate Pfizer governance cross-functional team(s).
They will regularly perform literature reviews and landscape assessments as directed for novel real world databases, registries and other relevant technologies stemming from patient advocacy, federal government, or other sources, and share these back with RWE leadership and other stakeholders. This role will also serve as a trusted expert for incorporating the voice of the patient into research and business evidence with key regulatory agencies (e.g., Clinical communities and professional societies who maintain evidence-based guidelines, FDA in the US, EMA in Europe, MHRA in the UK, PDMA in Japan, CDE in China), HTAs/Payers, and other stakeholders as needed. Finally they will help define and track success metrics and relevant KPIs as directed by the Head of Patient Advocacy and External Partnerships, then rapidly communicate their successes, publications, external speaking engagements, and lessons learned to the RWE Impact Translation lead.
ROLE RESPONSIBILITIES- Under supervision from their supervisor, develop execution plans to realize our vision for patient-centric RWE and inclusion of the patient voice in global, regional and local level for priority markets- Proactively partner with RWE Strategists, RWE Science & Epidemiology Leads, Clinical Scientists, Platforms & Partnerships and other colleagues to maximize inclusion of the patient voice where appropriate- Perform literature reviews and landscape assessments of novel real world datasets, registries and related deliverables from patient advocacy groups- Design studies to deliver cutting-edge research & lead external facing projects that expand Pfizer’s leadership in Patient & Public Involvement and Engagement (PPIE) from single market excellence to span across all 16 key “anchor” markets- Provide expert consultation as directed to inform patient advocacy groups’ RWE-related activities by sharing best practices, approaches and applicable common data models / data standards, where appropriate- Create executive summaries of opportunities from the literature, white papers, conferences and stakeholder events to bring back to the Platform and present in risk/benefits, required investment, and anticipated impact for our patients- Collaborates with CMAO and RWE Platforms & Partnerships colleagues, Clinical Scientists, Biostatistics, Statistical Programming and other parties as needed to achieve business and research goals- Supports the Head in building upon a team culture of continuous learning & objective measurements activities for end-to-end evidence generation
BASIC QUALIFICATIONS- Advanced degree, including MD, PhD or equivalent qualifications or demonstrated successful professional experience.-
- Direct experience as part of product development and/or access cross-functional teams- Ability to establish a vision and obtain buy-in and endorsement from cross-functional parties across the lifecycle- A high degree of energy, enthusiasm and motivation for scientific discoveries- Strong situational leadership skills & the ability to lead through influence in cross-functional & highly matrixed teams- Leadership in a related scientific field, e.g., in professional societies, government, international bodies, etc.- Global recognition as a scientific leader with e.g., 10+ scientific publications in peer-reviewed journals and conference proceedings in areas relevant for the ta
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