To coordinate with PI for IRB /IEC submission,notification
To supervise Site Feasibilities site qualification, visit management
To ensure that communication withSponsor/CRO/PI is prompt, adequate and timely
Prepare site for Site Selection Visit (SIV)
Prepare the Budget (PI/Sponsor/Institute) To ensure that all Case Report Forms (CRFs) and eCRFs are completed and all data queries withintimeline before all monitoring visits during the study are resolved within given timelines
Coordinate with physicians, hospital, coordinators schedules and other departments for scheduling thetrials and visits
To maintain and submit revisions & amendments of trials related documents to Ethics Committee
