1.Prepare, conduct and report on activities related to the completion of site selection, initiation, routine monitoring and close-out visits2.Monitor patient enrollment to ensure recruitment targets and project timelines are met at the site and/or country level3.Perform source data verification and follow up on data queries at the site level, on-going review of any 4.Risk Based Monitoring related information influencing data quality and frequency of site visits5.Ensure accurate and timely reporting and follow up of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations6.Act as the main line of communication between the Sponsor and the site.7.Be a point of contact/liaison for in-house support services and vendors.8.Ensure proper handling, accountability and reconciliation of all Investigational Product(s) and clinical study supplies9.Review the status and contents of essential documents at the site level and reconcile study OSF/ TMF at site and/or country level.10.Experience in all types of monitoring visits.