of HIV prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng primary, HIV, and gender-affirming health care services for key populations in the Johannesburg Health stakeholders and the Wits RHI Key Populations Programme team
of HIV prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng 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 the Key Populations Programme's senior management team, providing support to all activities and special
of HIV prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng 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 the Key Populations Programme's senior management team, providing support to all activities and special
job:
Required minimum education years’ experience in IT Support with managing teams
Desirable additional education
ensure protocol and GCP compliance
trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct, and 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 Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as needed
trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct, and 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 Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as needed