PURPOSE Senior Medical Manager (Sr. MM) is the in-house expertforthetherapeuticareas to which they are isassigned. Sr. MM acts as local medical representative and core member of the Therapeutic Area (TA) and Brand team, where they provide medical input and expertise for overall TA/Brand strategy, with comprehensive understanding of Medical/ Clinical environment, brand lifecycle needs and overall global and local medical objectives.

• Medicalstrategy development and implementation for effective lifecycle management • Responsiblefor development and execution of medicalstrategy of TA products to enable effective approval, access, and commercialization • Leadscross-functionalcolleagues and medical support for developing and implementing businessstrategiesandprograms • Planning and execution of medical initiatives (local advisory boards, scientific exchange meetings, medical lead symposia, etc.) in collaboration with medical team • Coordinate with medical team to communicate with HCPs based on medical strategies Medical leadership in creating scientific partnershipswithmedicalinstitutions,associations,medical key opinion leaders, etc • Manage scientificevents aligned with medical strategies • Medical leadership in product life-cycle management, collaborating with cross-functional team and riskmanagementconcerningsafetyissues • Review ofPromotionalactivities & mediarelease etc. as a medical reviewer • Provide internal scientific/medical training as a medical expert • Data Generation • Strategic planning of overarching of data generation plan for responsible TA/brand based on understanding of unmet scientific data and information needs • Lead collaboration with local study operations & RWE/NIS teams to successfully Initiate and manage local data generation activities (Protocol/synopsis development, Investigator selection & Investigator meetings, Study execution, results & publication, review of Investigator Sponsored Research (ISR) etc.) • Lead collaboration with cross functional teams for implementation of local non-interventional studies (NIS), management of post-marketing surveillance (PMS), and risk management plan (RMP); investigator-sponsored research (ISR) opportunities, and support for local feasibilities of phase clinical trials • In-House Medical Expert Role • Develop and maintain medical expertise in responsible therapeutic area • Participate as country representative in Glocal (Global-Local) Medical meetings, global study related meetings, etc. • Provide internal scientific/medical training as a medical expert • As Senior Medical Colleague; lead onboarding, training and development of junior Medical colleagues

• Medical degree or relevant scientific degree with specializationand/or appropriate experience in the required therapeutic area • Experience in the pharmaceutical industry, especially in Medical Affairs (5+ years preferred) • In-depth knowledge of responsible therapeutic areas and the relevant medicines, and ability to assess unmet needs of these fields • Comprehensive understanding of drug development process, including clinical research, regulatory approval, pricing & reimbursement, pharmacovigilance, etc. • Full understanding of compliance framework for medical activities in relation to local regulations and internal regulations, e.g. Pharmaceutical Affairs Law, KRPIA Code of Conduct, Pfizer Green Guide • Full understanding of the local health care policy and environment • Interest in a long-term career in the pharmaceutical industry • Ability to understand and critically evaluate clinical study protocols, reports, and scientific/medical publications • Strong managerial skills or potential • Ability to lead matrix teams • Highly developed interpersonal, communication, and collaboration skills • Fluency in Korean • Fluency in Business English

For more details, please refer to the company website.

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