I have 12 years of Industry experience into Pharmacovigilance.My Key Skills include:- Executing Pharmacovigilance Safety Management process - A combination of Case intake, Duplicate search, Triage, Case entry, Medical coding, Narrative writing, Case follow up- Proficient in using Global safety database: ARGUS, ARISg- Well versed with MedDRA and WHO Drug Dictionary- Expert in Case processing of Clinical trial, Non-interventional studies/programs, Literature, Spontaneous, Discharge summary and all Special situation cases.- SUSAR 7 day and 15 day safety package distribution for Open label, blinded and unblinded cases- Through knowledge of PSUR, DSUR, PBRER, PADER and RMP- Preparing Signal Evaluation Reports, Health Hazard Evaluations & Presenting Safety Signal data at SMT and SMC- Applying Scope & Methodology for Aggregate data analyses- Scheduling meetings & Prepare slides - Ensuring complete tracking, archiving, & miscellaneous administration of Signals from validation through Signal adjudication & Risk classification- Running reports, conducting preliminary analysis, & uploading reports in repository for medical review- Received WOW, OPEL, PLR, Star performer, Service Commitment & Best ICSR Awards- Quality oriented with Attention to details- Excellent Team player with ability to work in a Team environment - Manage, Plan and Organize work assignments and Work under strict timelines- Excellent Verbal and Written communication