Clinical Trial Coordinator
Current-Provide administrative and technical support to Project Team during the study-Provide administrative support for site activation and collect all needed Start-up documentation for the study-Work with different kind of program systems -Provide system support and ensure system database are always current and tasks are performed on time-Assist with compilation of Investigator Site File (ISF) and Pharmacy binder-Monitoring the study to ensure that it complies with protocol and is ethically-conducted -Daily communication with participants, PI's, Sub-I's, monitors, pharmacists and various departments of hospital-Collection, labeling, storage and transport of all specimens-Making sure that all equipment and supplies needed for the study are in-stock, not expired and in good condition