they can be replicated Develop and effectively manage relationships with external and internal stakeholders collection, analysis, learning and knowledge management from the Collaborative to support CATALYST Ensure assessments indicators Jointly develop a knowledge management context for QI briefs every 6 months with coaches members Support conducting and documenting data patient feedback system and form semiannual Experienced national and subnational decisionmakers, site managers, health care providers, youth and community advisory
performance areas: Screen patients and patient files and identify potential patients for research studies documentation (CRFs, source documents, etc.) in patient files Accurately report on stats of participants experience working in midwifery or with ante-natal clinics or programmes Good understanding of issues and work experience: At least 2 years experience in a clinical research environment Desirable additional education
performance areas: Screen patients and patient files and identify potential patients for research studies documentation (CRFs, source documents, etc.) in patient files Accurately report on stats of participants experience working in midwifery or with ante-natal clinics or programmes Good understanding of issues and work experience: At least 2 years experience in a clinical research environment Desirable additional education
participants from the community/Wits RHI study clinics into a study and conduct data collection and research schedule Support data extraction from clinic registers, patient records or other relevant data sources information about the study Liaise with the site manager, stakeholders and community members to identify and address or refer the queries to your line manager accordingly Establishing a relationship of trust recruited on daily basis to team leader or project manager Filing and archiving of participant informed consent
participants from the community/Wits RHI study clinics into a study and conduct data collection and research schedule Support data extraction from clinic registers, patient records or other relevant data sources information about the study Liaise with the site manager, stakeholders and community members to identify and address or refer the queries to your line manager accordingly Establishing a relationship of trust recruited on daily basis to team leader or project manager Filing and archiving of participant informed consent
participants from the community/Wits RHI study clinics into a study and conduct data collection and research schedule Support data extraction from clinic registers, patient records or other relevant data sources information about the study Liaise with the site manager, stakeholders and community members to identify and address or refer the queries to your line manager accordingly Establishing a relationship of trust recruited on daily basis to team leader or project manager Filing and archiving of participant informed consent
participants from the community/Wits RHI study clinics into a study and conduct data collection and research schedule Support data extraction from clinic registers, patient records or other relevant data sources information about the study Liaise with the site manager, stakeholders and community members to identify and address or refer the queries to your line manager accordingly Establishing a relationship of trust recruited on daily basis to team leader or project manager Filing and archiving of participant informed consent
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 sources as per study requirements/SOPs Collect, manage and maintain quality data for research and operations of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant accountability for tasks and demonstrates effective self-management Follow through to ensure that quality and productivity
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 sources as per study requirements/SOPs Collect, manage and maintain quality data for research and operations of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant accountability for tasks and demonstrates effective self-management Follow through to ensure that quality and productivity
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 sources as per study requirements/SOPs Collect, manage and maintain quality data for research and operations of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant accountability for tasks and demonstrates effective self-management Follow through to ensure that quality and productivity