Communicate as needed with Division of AIDS or DAIDS contractors. Manage clinical site laboratory supply program
corporate objectives and policies Guide organization personnel through new practices and certifications Supervise
Requires close collaboration with the regulatory personnel in the Sub-Saharan African region. Apply regulatory
timelines. Regular follow up with key SAHPRA personnel on the status of all outstanding approvals. Regular
timelines. Regular follow up with key SAHPRA personnel on the status of all outstanding approvals. Regular
timelines. Regular follow up with key SAHPRA personnel on the status of all outstanding approvals. Regular