responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
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 enrolment of eligible patients according to protocol requirements Compliance with all relevant SOPs Communicate Events of Medical Importance as per protocol requirements. Quality control of patient files and data entries
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 enrolment of eligible patients according to protocol requirements Compliance with all relevant SOPs Communicate Events of Medical Importance as per protocol requirements. Quality control of patient files and data entries
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 to achieve the 95-95-95 targets as per donor requirements
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 to achieve the 95-95-95 targets as per donor requirements Ensure compliance with Wits RHI, Department 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
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 to achieve the 95-95-95 targets as per donor requirements Ensure compliance with Wits RHI, Department 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
including operating systems, security tools, applications, servers, email systems, laptops, desktops, functional as well as staff and operational requirements are met
Required minimum education and training: