Serves as Pfizer Japan’s medical-scientific contact for HCPs and external stakeholders, shaping medical plans, exchanging evidence, supporting studies, and ensuring compliant use of medicines.
About this role
This staff role sits in Pfizer’s Japan Drug Safety Unit Case Management team and supports the handling of safety information for marketed and investigational products. The work covers individual case safety reporting within a broader pharmacovigilance and regulatory-compliance function, including activities connected with Japan, the United States and Europe.
The role collects and assesses adverse-event information, enters and manages records in the global safety database, responds to regulatory queries on individual safety reports, and contributes to internal and regulatory audits or inspections. It also participates in projects to develop global safety processes.
The posting identifies PC skills as required and specifies a medical qualification, such as registered pharmacist, or a science background at college level or above. Candidates must also be able to identify and solve routine work challenges constructively, make outcome-oriented decisions, meet departmental quality standards while achieving personal goals, and work as part of a team.
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