Experienced Clinical Pharmacist with a demonstrated history of working in the higher education industry. Skilled in Medical Case Management, Emergency Management, Pharmacovigilance, Clinical Research, and Patient Education. Strong healthcare services professional graduated from Kerala university of health sciences. As pharmacovigilance specialist     For queries resolution to entire team (SME), ·       Collation of data for PMO and preparation of PMO tool kit and dashboard ·       Training the new team members and prepare MOM. ·       Training material preparation along wth TA SME and Leads. ·       Audit preparations and Updating Project Control Book ·       Leave notification ·       Requesting for different access to associates as per their job role, SharePoint access request ·       Experience in coding of adverse reaction a with the help of MedDRA. ·       Experience in special situation cases (eg: Medication errors, of-label use). ·       Having knowledge on general follow up queries and sending follow up request ·       Maintain technical and industry knowledge by: Attending and participating in applicable company-sponsored training ·       Review and evaluate AE case information to determine required action to be taken based on client policies and procedures. ·       Responsible to review the information auto-populated from IRT to ARISg. ·       Write the narrative in a chronological order by using the respective available templates with the information reported without spelling and spacing errors. ·       Assess the Listedness/labeledness for the Adverse Events reported based on the Reference Safety Information (RSI) or Company Core Data Sheet (CCDS) as applicable. ·       Review each coded MedDRA term and WHODrug term to ensure accuracy and confirm coding status is resolved. ·       Attending and participating in applicable company-sponsored training ·       Training the new team members and prepare MOM. ·       Experience in triage, intake, case pro- cessing, narrative writing and quality review in and reporting of individual case safety re- ports (ICSR) of solicited and unsolicited cases. ·       Quality review of individual case safety reports (ICSR). ·       Perform validation check to ensure no important AE information is missed to enter in the Database. ·       Entry of individual case safety reports (ICSR) into the safety database including confirmation of duplicate check performed in IRT. ·       Experience in handling workflow and prior- utilization of cases across multiple workflow.