prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng (Total of 4 si design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement programme
prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng (Total of 4 sites) design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient
prevention/treatment and complementary services in Western Cape, Vhembe, Ekurhuleni, and Gauteng (Total of 4 sites) design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient
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 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 minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education