· 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 · Experience should include monitoring skills. Prior relevant active independent field monitoring experience and site management experience