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 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 Support translation and transcription of qualitative data if required Adhere to Good Clinical Practice Standards
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate 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 Support translation and transcription of qualitative data if required Adhere to Good Clinical Practice Standards
and selectively record anatomical images, physical data and real time physiological information for health and generate reports, capturing data and images into an electronic data capture system Must be able to
and selectively record anatomical images, physical data and real time physiological information for health and generate reports, capturing data and images into an electronic data capture system Must be able to
matters.
standards. Approving, maintaining, and accurately capturing and authorizing any changes to manufacturing master re-occurrence of incidents. Ensuring all necessary data, training of personnel and applicators, and health
analysis of data, and publish scientific articles
conduct analysis of data, and publish scientific articles Enhance routine programme data analytics to inform team and other relevant staff Supervise fieldwork (data collection, interviews, etc.) Screen participants Extract data from participant medical records Conduct data collection and data quality processes Data management Storage and archiving of data according to SOP's (electronic and hard copy data) Adherence to study protocols reporting requirements Conduct data analysis according to agreed data analysis plan and write up results