identifying and briefing appropriate trial investigators (clinicians)
setting up and disbanding trial study centres
designing trial materials and supplying study centres with sufficient quantities
providing clinicians with instructions on how to conduct the trials
collecting and authenticating data collection forms (commonly known as case report form
monitoring progress throughout the duration of the trial
writing reports
Planning the requirements for clinical trial material, ordering clinical trial material (head office or local comparators), setting up and monitoring the systems whereby the Clinical Research Assistant can ship CT material to the investigator, maintaining procedures to account for the CT material, checking the expiration of CT material and requesting extensions if necessary.
