Sr. Medical Affairs Scientist（1 Year Fixed Term）
Sr. Medical Affairs Scientist (MAS) main role is to create and implement strategies, to build and develop enduring peer-to-peer relationships with healthcare professionals and institutions, creating constructive, cross-functional partnerships with internal and external stakeholders to generate customer insights and leverage business opportunities. This role will be to provide medical support that is aligned and integrated to the overall strategy within Hospital Anti-Infective Therapeutic Area (TA) brand operating and clinical plans.
As a Customer Facing Medical role, create and implement strategies to build and develop enduring peer-to-peer relationships with healthcare professionals (HCPs) and institutions, and create cross-functional partnerships with internal and external stakeholders through scientific communication to gather customer intelligence and insights and leverage business opportunities
Ensure effective customer and medical/clinical environment mapping to guide in Medical interactions
Create Medical to Medical Interaction Plan & actively interact with in individual scientific leaders in the field
Support the creation of partnerships with relevant Medical Societies, government agencies, and other industry groups
Exchange high-quality, accurate, well-balanced, and directed scientific information with customers and stakeholders in response to unsolicited medical requests
In response to unsolicited medical requests for information, communicating scientific data on TA portfolio including off label indications and on compounds in development where specifically requested
Ensure customer intelligence and insights are fed back into organization to aid internal strategies and leveraging of business opportunities
Act as bridge between Pfizer scientists and other internal resources and external HCP and independent researchers to facilitate scientific collaborations
Support Medical and Brand Strategies
Development/ implementation of strategy, tactics and operating plan at country level to ensure plans are successfully developed and executed to achieve short- and long-term objectives in alignment with global, regional and local medical and brand goals
In compliance and close coordination with medical team/ Medical Lead, develop and implement key medical projects and initiatives to enhance proper dissemination of medical and scientific information
Collaborate with team; (Sr.) Medical Manager, Medical Lead in management of medical initiatives including local advisory boards, scientific exchange meetings, medical lead symposia, etc.
Collaborate with (Sr.) Medical Manager/Medical Lead and communicate with HCPs based on medical strategies by initiation and implementation of local non-interventional studies (NIS), management of post-marketing surveillance (PMS), and risk management plan (RMP); investigator-sponsored research (ISR) opportunities; support for local feasibilities of phase 1-4 clinical trials
Medical leadership and insight for crossfunctional initiatives; medical input for regulatory, access, commercial etc. initiatives
Support collaborations internally with commercial TA teams; internal training, medical input for material review, etc.
Support Data Generation
Collaborate with local study operations & RWE/NIS teams for successful data generation through non-interventional studies including regulatory post marketing surveillance
Support coordination & investigator communications for Investigator Sponsored Research (ISR), Research Collaborations (CRC) & CTP (Compound Transfer Programs)
Develop and maintain medical expertise in responsible therapeutic area
Act as Customer Facing Medical Role expert; supporting onboarding, training and development of MA Scientist (MAS) as needed
Hospital portfolio medical management
Support Medical Lead and/or (Sr.) Medical Manager to evaluate the medical necessity of products periodically and ensure the appropriateness of updating product label as a medical expert.
Provide medical insights to support product supply management and proper decision.
REQUIRED SKILLS
Medical, pharmacy, veterinary medicine, nursing, life science or other relevant advanced degree
Experience in Medical Affairs and/or Customer Facing Medical role (3+ years preferred)
In-depth knowledge of responsible therapeutic areas and the relevant medicines
Good understanding of drug development process, including clinical research, regulatory approval, pricing & reimbursement, pharmacovigilance, etc.
Good 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
Good understanding of the local health care policy and environment
Ability to understand and critically evaluate clinical study protocols, reports, and scientific/medical publications
Highly developed interpersonal, communication, and collaboration skills
Fluency in Korean
Fluency in business English strongly preferred
Application Deadline: 6pm, 21st, April (Mon), 2025
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
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