Clinical Trail Management can involve thousands of people, hundreds of investigative sites, multiple CROs and various clinical source systems – all generating huge amounts of data. Our Clinical research associates overseas the each study of the clinical process to ensure proper planning, conduct, patient safety, data quality. Clinical trail Management is a site management which requires the maximum no. Of subjects. Our CTM is a powerful end-to-end clinical trial management solution that provides control, efficiency and quality data to every study For this process they require Clinical Research Associate (CRA) which takes a major part.CRA major work is to gather, collect and maintain all the subjects information manually.