Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH GCP guidelines.

Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of
clinical trials, and close clinical trials at investigative sites.

Reviews and verifies accuracy of clinical trial data collected, either on site or remotely.

Provides regular site status information to team members, trial management, and updates trial management tools,

Completes monitoring activity documents as required by SOPs or other contractual obligations.

Works closely with other clinical team members to fa...