design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming populations in the Johannesburg Health District
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming populations in the Johannesburg Health District Monitor and review the implementation and progress of site Wits RHI Key Populations Programme team Regularly monitor and track site performance in relation to programme with senior management, control and monitor expenditures of the clinic, adhering to relevant finance and policies, contracts, and agreements Support the monitoring, evaluation & recording of outputs to evaluate
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming populations in the Johannesburg Health District Monitor and review the implementation and progress of site Wits RHI Key Populations Programme team Regularly monitor and track site performance in relation to programme with senior management, control and monitor expenditures of the clinic, adhering to relevant finance and policies, contracts, and agreements Support the monitoring, evaluation & recording of outputs to evaluate
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Desirable
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor key meetings to manage the study Manage site monitoring visits/audits or similar Manage procurement for minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor key meetings to manage the study Manage site monitoring visits/audits or similar Manage procurement for minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education