of HIV prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng Sex Workers and Transgender”
of HIV prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng Populations, Sex Workers and Transgender” Lead the technical design, implementation and continuous improvement primary, HIV, and gender-affirming health care services for key populations in the Johannesburg Health stakeholders and the Wits RHI Key Populations Programme team Regularly monitor and track site performance in implementation challenges and work with the appropriate team leads to develop, resource and implement corrective
of HIV prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng Populations, Sex Workers and Transgender” Lead the technical design, implementation and continuous improvement primary, HIV, and gender-affirming health care services for key populations in the Johannesburg Health stakeholders and the Wits RHI Key Populations Programme team Regularly monitor and track site performance in implementation challenges and work with the appropriate team leads to develop, resource and implement corrective
job:
Required minimum education years’ experience in IT Support with managing teams
Desirable additional education personal abilities:
protocol and GCP compliance
ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants events Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform
ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants events Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform