• Manage the receipt and processing of all adverse event report ( exp. Spontaneous case, Literature case, posts authorization safety study, post marketing surveillanceperform clinical checks, search data base to prevent duplicate entries (Argus) and processing various E2B reports.• Coding of company suspect drug with company drug dictionary (CDD) and review coding of other company suspect drugs, concomitant product, past and treatment drugs using WHODD.• Coding of following fields using the most appropriate lower level term (LLT) from medDRA, like medical history, reported adverse event, lab data and procedures.• Determine expectedness and causality.• Write and review case narrative.• Processing literature case from reading through the abstracts, citations and full publication.