Sr. Medical Affairs Scientist（1 Year Fixed Term）

• 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