will be responsible for participant recruitment and data collection at the allocated study sites
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
from the community/Wits RHI study clinics into a study and conduct data collection and research intervi schedule
from the community/Wits RHI study clinics into a study and conduct data collection and research intervi schedule
from the community/Wits RHI study clinics into a study and conduct data collection and research interviews schedule Support data extraction from clinic registers, patient records or other relevant data sources as per with recruited study participants Support data capture and data quality control on sites Engage with stakeholders to resolve questions, inconsistencies, or missing data Chair or take minutes of relevant meetings i.e. materials (HREC approved) on site Identify missing data, inconsistencies and/or errors and follow up or