Clinic Applications Administrator Jobs in South Africa
- Gauteng (12)
- Kwazulu Natal (8)
- North West (7)
- Western Cape (3)
- Limpopo (1)
- Free State (1)
Aj Personnel
- Contract
- Last 7 days (10)
Research Study Assistant (3 Months Fixed Term Contract Mthatha Wits Rhi)
Aj Personnel
South Africa
participants from the community/Wits RHI study clinics into a study and conduct data collection and research interviews Contribute towards ongoing monitoring and administration of the study Participate in the process of discussions and distributing study information (as applicable) at study sites and/or in communities Address to study schedule Support data extraction from clinic registers, patient records or other relevant data relevant documentation and place in files (if applicable) Take ownership and accountability for tasks
share this job on whatsappResearch Study Assistant (3 Months Fixed Term Contract Tshwane Wits Rhi)
Aj PersonnelSouth Africa
participants from the community/Wits RHI study clinics into a study and conduct data collection and research interviews Contribute towards ongoing monitoring and administration of the study Participate in the process of discussions and distributing study information (as applicable) at study sites and/or in communities Address to study schedule Support data extraction from clinic registers, patient records or other relevant data relevant documentation and place in files (if applicable) Take ownership and accountability for tasks
Research Study Assistant Mthatha, South Africa
Aj PersonnelSouth Africa
participants from the community/Wits RHI study clinics into a study and conduct data collection and research interviews Contribute towards ongoing monitoring and administration of the study Participate in the process of discussions and distributing study information (as applicable) at study sites and/or in communities Address to study schedule Support data extraction from clinic registers, patient records or other relevant data relevant documentation and place in files (if applicable) Take ownership and accountability for tasks
Research Study Assistant Pretoria, South Africa
Aj PersonnelSouth Africa
participants from the community/Wits RHI study clinics into a study and conduct data collection and research interviews Contribute towards ongoing monitoring and administration of the study Participate in the process of discussions and distributing study information (as applicable) at study sites and/or in communities Address to study schedule Support data extraction from clinic registers, patient records or other relevant data relevant documentation and place in files (if applicable) Take ownership and accountability for tasks
Fieldworker Hillbrow, South Africa
Aj PersonnelHillbrow
also contribute towards ongoing monitoring and administration of the designated studies; participate in the participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
Fieldworker Pretoria, South Africa
Aj PersonnelSouth Africa
also contribute towards ongoing monitoring and administration of the designated studies; participate in the participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
Fieldworkers (x 4 Three Months Fixed Term Contract Mthatha Wits Rhi)
Aj PersonnelSouth Africa
also contribute towards ongoing monitoring and administration of the designated studies; participate in the participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
Fieldworkers (x2 Three Months Fixed Term Contract Hillbrow Wits Rhi)
Aj PersonnelHillbrow
also contribute towards ongoing monitoring and administration of the designated studies; participate in the participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
Fieldworker Mthatha, South Africa
Aj PersonnelSouth Africa
also contribute towards ongoing monitoring and administration of the designated studies; participate in the participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
Fieldworkers (x4 Three Months Fixed Term Contract Tshwane Wits Rhi)
Aj PersonnelSouth Africa
also contribute towards ongoing monitoring and administration of the designated studies; participate in the participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
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