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**Job Description** Specific Responsibilities + Reviews adverse reports received for marketed and investigational products, adhering to standard operating procedures for medical assessment of individual case safety reports providing safety assessment and pharmacovigilance comment + Performs quality control (QC) of adverse event reports from a medical review perspective + Participates in both internal and external educational initiatives + Initiate, lead, or contributes to a functional or cross-functional project + Participates in process improvement initiatives by identifying areas for improvement and presents solutions + May serve on higher level intradepartmental and interdepartmental cross-functional projects + May le...