Evaluation,prioritizatiozion and processing of adverse events in the global safety database within agreed timeframe and to a high standard of accuracy in compliance with standard operating procedures and global regulatory requirements.Performing duplicate, check for valid cases as per client requirements, consistent data entry and processing from source documents adhering to timelines and quality .Confirm consistent coding of medical history and adverse events.Assesing ADR for labelling including USPI.

1.Assisting with preparation and submission of clinical trial documents, maintained study files and ensured that they were up-to-date and organized.2.Participated in Site Initiation Visit, Monitoring visits and Site Closeout visit.3.Conducting study related tasks such as Patient screening, enrollment, Data collection and entering into EDC.4.Contributed to Data analysis and reporting.5.Providing support to study coordinator and Investigator by helping with study related tasks such as Data entry, filing and Protocol related things.