.Responsible to plan, initiate, develop and organize clinical trials in accordance to the highest standards required in ICH E6 GCP, local GCP, regulatory compliance, data integrity and compliance with the study requirements .Responsible to lead and motivate project team(s) on all project-related issues to ensure all activities are conducted in highest quality standards, in compliance with ICH E6 GCP, local GCP and applicable local regulatory requirements as well as to meet/exceed sponsor''''s expectation .Responsible to supervise daily operations and management of activities associated with assigned project(s) from concept to completion of final study report and ensure project goals are achieved .Responsible to lead project team(s), sponsor and vendors, pertaining to logistics management, clinical supplies and investigational product logisitics, systems set up and/or any other requirements, are in place to ensure swift study start up