Acquire details of the clinical trial, patient population, specific inclusion and exclusion criteria, and lab work required throughout the testing
Monitor the generated data files for the patients tested on a weekly basis
Coordinate the collection and shipment of blood samples within the clinical site, and between the clinical site and labs testing the samples
Coordinate adverse events and deviations and inquiries required to close the clinical trial
Coordinate the final clinical report required for regulatory submission.
ClinCore may also assign a Client Manager and Clinical Site Manager to coordinate and document the events between the sponsor and clinical site. This is to ensure accurate execution of the clinical protocol, approved for the testing of the drug in that clinical phase, and to allow the regulatory submission at the end of the trial.