the clinical trial to ensure protocol and GCP compliance
the clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up start-up, conduct, and close-out Manage regulatory updates throughout the study (New ICFs, Protocol Amendments Assistants Communicate with CRO, Sponsor, and regulatory authorities regarding notifiable trial events eligible patients according to protocol requirements Compliance with all relevant SOPs Communicate well with systematic in approach to tasks, with strict compliance to protocols Exceptional organizational and administrative
the clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up start-up, conduct, and close-out Manage regulatory updates throughout the study (New ICFs, Protocol Amendments Assistants Communicate with CRO, Sponsor, and regulatory authorities regarding notifiable trial events eligible patients according to protocol requirements Compliance with all relevant SOPs Communicate well with systematic in approach to tasks, with strict compliance to protocols Exceptional organizational and administrative
targets as per donor requirements
95-95-95 targets as per donor requirements Ensure compliance with Wits RHI, Department of Health and USAID
95-95-95 targets as per donor requirements Ensure compliance with Wits RHI, Department of Health and USAID