●Started working as full data entry associate responsible for executing efficient coding for Products, events, medical history, medications, and tests, alongside crafting engaging narratives.● Ensuring completeness and accuracy and enhance regulatory reportability by entering data into the safety database.● Accomplished prompt processing of various case types including clinical trial, spontaneous(BP/HA/Social media), observational cases, PSP/PAP, market research program and medical device cases.

● Started my career as an Intake and Assessment associate, responsible for prioritizing cases while assessing ICSR for case validity ( Initial, Follow-up, Duplicate, and Non-case), seriousness and raising urgent queries for discrepancies and other related activities.●Developed expertise in utilizing various functionalities of the LSMV database over time, including QBE, various report generation, and compare and reconcile.●Performed mentoring of newly joined associates, Late Case Analysis (LCA), case deletion reviews and preparing Excel sheets for internal and external quality assessments.