Medical Affairs Scientist New

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ROLE SUMMARY
  • The Medical Affairs Scientist (MAS) is a key scientific ambassador for Pfizer, building long-term partnerships with healthcare professionals (HCPs), key opinion leaders (KOLs), and other stakeholders to advance patient outcomes. Operating at the intersection of science, healthcare innovation, and patient impact, as a MAS, your role is central to the success of medical affairs in the Country Cluster Structure.

MAIN REPONSIBILITIES / DUTIES

Insight Generation, Synthesis & Sharing
  • Engage with HCPs, KOLs, authorities, and scientific stakeholders as a peer, fostering trust and credibility in all
interactions.
  • Generate, document, synthesize, and compliantly share actionable medical insights from external engagements,
scientific exchange, and stakeholder feedback.
  • Effectively disseminate key scientific insights using omnichannel and digital platforms, ensuring relevant
information reaches stakeholders in a timely and accessible manner.
  • Ensure insights are communicated effectively to cluster medical leadership, cross-functional teams, and relevant
internal stakeholders to inform strategy, tactics, and operational plans.
  • Support the Country Medical Lead (CML) in external engagement, acting as a visible and credible representative

of Pfizer Medical in the market.

External Engagement & Stakeholder Management
  • Formulate and execute a prioritized and impactful medical plan, including KOL mapping. Use metrics to learn
and iteratively improve.
  • Execute, manage and lead local projects, events and omnichannel activities in alignment with cluster and
International strategy and plans.
  • Build and optimize enduring relationships with external stakeholders, including medical societies, regulators,
patient advocacy groups, and payors.
  • Actively participate in external forums and scientific events, representing Pfizer’s medical interests and supporting the CML’s leadership in these settings.
  • Serve as a scientific point of contact for assigned therapeutic areas in-country, collaborating with above country cluster Scientific Experts and other internal stakeholders.
  • Targeted support of the local clinical trial environment including protocol feasibility, site identification, investigator engagement, and supporting recruitment.
Collaborative Working
  • Compliantly share stakeholder insights internally to identify collaboration opportunities and drive cross-functional alignment.
  • Collaborate with cluster medical, access, regulatory, clinical, and commercial teams to support integrated planning and execution.
  • Inform and contribute to the execution of cluster-level medical and brand strategies in alignment with global and International goals.
Operational Effectiveness & Compliance
  • Uphold the highest ethical standards, scientific integrity, and compliance in all activities.
  • Take responsibility for own learning, ensuring your skills and knowledge are up to date.
  • Support regulatory and pharmacovigilance departments for compliance activities (safety updates, product supply issues, etc.).
REQUIRED SKILL SET
  • Advanced healthcare or scientific degree coupled with deep pharmaceutical experience and knowledge. A

medical degree (MD) or equivalent and board certification, or TA-related PhD and post-doctoral experience is

desirable.
  • Robust scientific and medical experience, including clinical or research experience.
  • Knowledge of the pharmaceutical industry, local healthcare systems, and regulatory environments.
  • Demonstrated ability to analyze medical data and generate insights.
  • Fluent business and medical English (additional languages as required by market).
STAKEHOLDER MANAGEMENT
  • External Stakeholders: Healthcare professionals (HCPs), including physicians, pharmacists, and clinical

investigators; Key Opinion Leaders (KOLs) and scientific experts in assigned therapeutic areas; Medical

societies, professional associations, and academic institutions; Regulatory authorities, payors, and government

health agencies; Patient advocacy groups and relevant non-governmental organizations; Contributors to

national formularies.
  • Internal Stakeholders: Country Medical Lead (CML), supporting external engagement and strategic initiatives;
Cluster Scientific Experts; Cross-functional teams: Access & Value, Regulatory, Clinical Operations, Commercial,

and Brand Teams; Cluster medical leadership and international medical colleagues.

RESOURCES MANAGED
  • Financial Accountability: The MAS may contribute to budget planning and oversight for medical initiatives, scientific events, and evidence generation activities, working collaboratively with the Country Medical Lead and cross-functional teams to ensure resources are used efficiently to maximize patient and business impact.
  • People Management:

This role is an individual contributor.

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