submission to the study coordinator/leadership team Assist in patient recruitment, screening, enrolment, and according to protocol requirements as and when required Assist with stock-take for the project, ensuring stock maintained and low stock is flagged for procurement Assist the team with ad hoc assignments and duties as
Introduction The Wits Reproductive Health and HIV Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health challenges. It is located within the University of the Witwatersrand and addresses some of the greatest public health concerns affecting our reg
to the study coordinator/leadership team
monitoring reviews Assist in the completion of corrective action for monitoring reviews Assist/ensure completion documentation available and up to date across all studies Assist with the review and revision of standard operating
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
biological specimens from participants, conduct basic analysis according to protocol, and send samples
submission to the study coordinator/leadership team Assist in patient recruitment, screening, enrolment, and according to protocol requirements as and when required Assist with stock-take for the project, ensuring stock maintained and low stock is flagged for procurement Assist the team with ad hoc assignments and duties as
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
trial to ensure protocol and GCP compliance
monitoring reviews Assist in the completion of corrective action for monitoring reviews Assist/ensure completion documentation available and up to date across all studies Assist with the review and revision of standard operating