Senior Director International Internal Medicine Antiviral non-MD

ROLE SUMMARY

This position assumes a leadership role within Internal Medicine and Primary Care in International) Medical Affairs to support medical affairs activities for international countries with primary responsibility as the lead medical and scientific expert for the Antiviral Disease area and portfolio. The role will act as one of the medical specialists leading scientific work on specific product/(s) to provide medical leadership strategy and support for international countries in alignment with Global Strategy. He/She is the medical voice of the antiviral portfolio combining medical expertise and understanding of the patients and physicians point of view with indepth knowledge . He/She will lead with integrity and be a role model for medical professionalism and scientific excellence. This will be achieved by crossfunctional integration with stakeholders at global international and local levels (e.g. research and development health outcomes commercial regulatory safety public affairs); lead of evidence and insight generation interpretation and dissemination activities for the safe and effective use of antiviral assets; coordinating work and strategies where appropriate with KOLs and external scientists; conducting and publishing results of high quality scientific studies of relevance to asset goals; represent Pfizer at key regional meetings global meetings and scientific congresses.

For this international posting geographic focus will be on Europe Middle East and Asia based key markets. Candidates need to be able to manage these time zones.

ROLE RESPONSIBILITIES

Accountable for ensuring integration of scientific information (epidemiology disease burden public health value etc. in communication materials for the assigned asset(s) or disease area to maximize patient access and benefits.

Acts as a subject matter expert on specified asset(s) and disease area science within and outside of Pfizer.

Manages product(s) within the antiviral portfolio across their lifecycle.

Provides matrix leadership for assigned international country teams.

Contributes to the development of international strategies for publications scientific congresses and advisory boards in support of scientific data related to asset(s) and disease area.

Identifies establishes and maintains relationships with external partners that can inform on scientific issues of relevance to asset(s) policies and decisionmaking.

In partnership with country Medical Affairs colleagues leads or participates in the cocreation of Global medical to medical content that will be delivered to countries as well as materials for promotion congresses and symposia in full compliance with Pfizer policy.

Joins relevant Global &International Country workstreams if applicable (e.g. international member of GMAT or the Scientific Publication Committee (SPC)

Leads the scientific dialogue and positioning of antiviral asset(s) and related science in International including but not limited to:

• Gaining insights from medical advisory boards in accordance with Pfizer policies and procedures.
• Providing credible and accurate scientific data demonstrating the value of assigned product(s) and differentiating them from other medicines to support country level tendering processes.
• Assisting with competitive intelligence for assigned asset(s) including gathering and communicating findings.

Oversees collection and integration of published scientific data necessary for developing product labels.

Reviews international external grant proposals as member of the Medical Scientific Committee

Contributes as a member of the assigned category Leadership Team

Supports development of strategies for clinical studies and trial

Provides the needed support to country medical teams in the organization of medical education events maintains professional scientific relationships with external opinion leaders & interacts with health care professionals as applicable

Contributes to the planning and timely highquality of medical tactics to support the country(ies) and lifecycle plan.

Creates asset related community groups across international medical affairs colleagues to enhance learning/best practice sharing.

Works closely with Global MA Teams and platform functions to develop and implement omnichannel medical strategy in alignment with commercial regional offices.

Supports country or regional medical interactions with local regulatory authorities and KOLs as needed

BASIC QUALIFICATIONS

• PharmD/PhD: At least 7 years of relevant experience in the pharmaceutical industry.
• Subject matter expertise and experience in Antiviral or related area.
• Demonstrated ability to develop lead and execute global medical affairs strategies and tactics including data generation data dissemination and medical education
• Experience with patient care especially in specific therapeutic area preferred.
• Deep understanding of HCP informational needs and what is required to support these needs.
• Extensive knowledge of patterns of medical practice and healthcare delivery and current and evolving landscape will be required.
• Demonstrated experience designing and overseeing implementation of clinical interventional or noninterventional studies including methodology analytic plans interpretation and budgets and conducting onsite assessments of study progress.
• Proven ability to interact with senior KOLs and Government officials.
• Demonstrated experience effectively leading and collaborating with matrixed teams
• Established track record of valued and compliance leadership including across diverse cultures and geographies.
• Documented ability to take an assetrelated project from start to end including conception design protocol analytic plan implementation analysis and reporting and interpretation of results.
• Able to review evaluate interpret and present complex data; understand information on emerging safety and efficacy profile of related asset(s).
• Understand the critical data elements related to access process (including from clinical development programs and HTA analysis approaches of different reimbursement bodies) and lead the data generation process in IDM countries in alignment with these.
• An ability to lead and manage in a matrixed structure and in a collaborative team environment. Demonstrated ability to think and act strategically.
• Demonstrated record of sound judgment and intelligent decisionmaking.
• Excellent verbal and written communication skills including scientific writing skills.
• Strong work ethic and history of delivering project within stated timelines.
• Reliability organizational skills compliance mindset.

Work Location Assignment:Hybrid