Support the tasks below for assigned project throughout the study:
Requests payments in ACM/Ariba for study related cost
Updates the trial and site information as necessary in Corporate Clinical Trial Registry (CCTR) in a timely manner
Attends appropriate training programs and project teleconferences as applicable.
Maintains the study status tracking and provides analysis report to Study Manager.
Assists Study Manager on study budget control by timely tracking and reporting of actual cost and forecast drafting.
Coordinates Clinical Study Agreement approval to ensure site initiation on time.
Study Start-Up o Supports and coordinates the clinical trial application to ethics committee and regulatory authority, if applicable, to obtain approval within required timeline. o Coordinates and applies for export/import license of, lab kits...