Collects and assesses adverse-event information for marketed and investigational products, manages global safety-database data, supports regulatory compliance and inspections, and answers case-report queries.
About this role
This medical affairs role sits in Pfizer Japan’s oncology organization for lung cancer. It is the medical and scientific contact for healthcare professionals, medical societies, regulators, academia, and other external stakeholders, linking local planning with global strategy and evidence-based product use.
Core work is to identify unmet medical needs and data gaps, develop and execute medical plans, conduct non-promotional scientific exchange, organize advisory boards and educational programs, and bring stakeholder insights into strategy. The role also supports clinical-trial protocol feasibility, investigator and site identification, real-world evidence, non-interventional and database studies, registries, publications, medical materials, safety reporting, and clinical-development activities.
Applicants must meet a stated education route: a four-year university degree plus a life-science master’s; specified pharmacist qualifications; a nurse’s master’s degree; or qualification as a veterinarian, dentist, or MD. Relevant medical or pharmaceutical expertise, stakeholder communication, and cross-functional collaboration are required.
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