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職責(zé)描述： · 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 任職要求： · Strong knowledge in ICH-GCP · Ability to review and evaluate clinical data · Computer literacy desirable · Good oral and written communication skills · Due to the nature of this position it may be required for the employee to travel · Bachelor degree, or local equivalent, in medicine, science or related discipline