◦Act as the main line of communication between the sponsor and the investigator◦Verifying that all research staff, facilities and investigational products have adequate qualifications and resources and these remain adequate throughout◦Responsible for the safety and proper conduct throughout the trial◦Verifying that the investigator follows the approved protocol and all GCP procedures◦Verifying that source data/documents and other trial records are accurate, complete, and maintained◦Adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol on the CRFs◦Communicating deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator

Head Research Nurse for Clinical Trials