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
Within Pfizer Japan’s Medical Affairs organization, this field medical role is the scientific contact for healthcare professionals, medical societies, regulators, academia and other external stakeholders. It contributes to medical strategy, clinical planning and evidence generation for assigned therapeutic areas.
The work includes stakeholder mapping, scientific exchanges, advisory boards, educational seminars, medical materials, unsolicited medical requests, investigator-sponsored research and grants. It may also support real-world evidence, non-interventional studies, database studies and registries, while bringing external insights into cross-functional decisions. The minimum qualification is a four-year university degree plus a master’s in life science, or an accepted pharmacist, six-year pharmacy, nurse-with-master’s, veterinarian, dentist or MD pathway; specified equivalent life-science research experience may qualify.
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