The detail activitiy as below : 1. Site selection : Evaluate site qualilification to select qualified site for clinical trial.
2. Site Initiation : Communicate with site staff to obtain EC approval and signed CTAg and provide study training to site staff.
3. Monitoring visit : Conduct monitoring according to GCP, protocol and BMS SOP requirement to ensure study quality. 4. Site closure : Follow study timeline to close site.
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