Clinical Research Associates Jobs in South Africa - Page 3
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Research Study Assistant (3 Months Fixed Term Contract Tshwane Wits Rhi)
Aj Personnel
South Africa
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health community/Wits RHI study clinics into a study and conduct data collection and research interviews Contribute appointments with eligible participants to attend research interviews at identified study sites Conduct Informed to study schedule Support data extraction from clinic registers, patient records or other relevant data abreast with working trends by conducting weekly Clinic visits and assisting patients and caregivers Participate
share this job on whatsappRa Associate / Ra Officer (pharmaceutical). 1-year Contract. Jhb South. R25 - R30k P/m. R25 - R30k P/m
Specialist Search RecruitmentSouth Africa
R25 - R30k p/m sector has an opportunity for an experienced RA Associate / RA Officer to assist the RA team. You need one one full year of RA Officer / RA Associate experience within the regulatory affairs department at a pharmaceutical experience as a Regulatory Affairs Scientist / RA Associate and/or RA Officer. A working knowledge of the have at least one full year of RA Officer / RA Associate experience at a PHARMACEUTICAL company to apply
Care Coordinator Kwazulu-natal (pietermaritzburg, Newcastle, Lady Smith, Eshowe, Richards Bay, Empangeni)
Ppo ServeSouth Africa
us to change the health care system using your clinical knowledge and organisational skills. You must precisely, iterate, be lean, and prove yourself. Your clinical knowledge must be sound. You must be able to challenge admin staff) Assistance in the documentation of clinical information Maintain relationships between external improvement. Clinical process development: Understanding clinical process and engage with clinical data to understand the issues Provide clinical input into broad range of clinical developmental work including
Care Coordinators Market Related
Ppo ServeSouth Africa
us to change the health care system using your clinical knowledge and organisational skills. You must precisely, iterate, be lean, and prove yourself. Your clinical knowledge must be sound. You must be able to challenge admin staff) Assistance in the documentation of clinical information Maintain relationships between external improvement. Clinical process development: Understanding clinical process and engage with clinical data to understand the issues Provide clinical input into broad range of clinical developmental work including
Fieldworker Hillbrow, South Africa
Aj PersonnelHillbrow
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health 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 Collect, manage and maintain quality data for research and operations purposes. Capture data into study of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant
Fieldworker Pretoria, South Africa
Aj PersonnelSouth Africa
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health 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 Collect, manage and maintain quality data for research and operations purposes. Capture data into study of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant
Fieldworkers (x 4 Three Months Fixed Term Contract Mthatha Wits Rhi)
Aj PersonnelSouth Africa
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health 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 Collect, manage and maintain quality data for research and operations purposes. Capture data into study of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant
Fieldworkers (x2 Three Months Fixed Term Contract Hillbrow Wits Rhi)
Aj PersonnelHillbrow
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health 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 Collect, manage and maintain quality data for research and operations purposes. Capture data into study of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant
Fieldworker Mthatha, South Africa
Aj PersonnelSouth Africa
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health 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 Collect, manage and maintain quality data for research and operations purposes. Capture data into study of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant
Fieldworkers (x4 Three Months Fixed Term Contract Tshwane Wits Rhi)
Aj PersonnelSouth Africa
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health 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 Collect, manage and maintain quality data for research and operations purposes. Capture data into study of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant
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