Scientist

• Engage with HCPs, KOLs, authorities, and scientific stakeholders as a peer
• Generate, document, synthesize, and compliantly share actionable medical insights
• Disseminate scientific insights through omnichannel and digital platforms
• Communicate insights to cluster medical leadership and cross-functional teams
• Support the Country Medical Lead in external engagement
• Formulate and execute prioritized medical plans, including KOL mapping
• Execute and lead local projects, events, and omnichannel activities
• Build relationships with medical societies, regulators, patient advocacy groups, and payors
• Represent Pfizer Medical at external forums and scientific events
• Serve as scientific point of contact for assigned therapeutic areas in-country
• Support the local clinical trial environment through protocol feasibility, site identification, investigator engagement, and recruitment support
• Collaborate with medical, access, regulatory, clinical, and commercial teams
• Contribute to cluster-level medical and brand strategies
• Uphold ethical, scientific integrity, and compliance standards
• Support regulatory and pharmacovigilance compliance activities

Medical Affairs Scientist

• Engage with HCPs, KOLs, authorities, and scientific stakeholders as a peer
• Generate, document, synthesize, and compliantly share actionable medical insights
• Disseminate scientific insights using omnichannel and digital platforms
• Communicate insights to medical leadership, cross-functional teams, and internal stakeholders
• Support the Country Medical Lead in external engagement
• Formulate and execute prioritized medical plans, including KOL mapping
• Execute and lead local projects, events, and omnichannel activities
• Build relationships with medical societies, regulators, patient advocacy groups, and payors
• Represent Pfizer’s medical interests at external forums and scientific events
• Serve as scientific point of contact for assigned therapeutic areas in-country
• Support the local clinical trial environment, including protocol feasibility, site identification, investigator engagement, and recruitment
• Collaborate with medical, access, regulatory, clinical, and commercial teams
• Contribute to cluster-level medical and brand strategies
• Uphold ethical standards, scientific integrity, and compliance
• Maintain current skills and knowledge
• Support regulatory and pharmacovigilance compliance activities