Wits Health Consortium (Pty) Limited (WHC) is a wholly-owned Company of the University of the Witwatersrand Johannesburg (South Africa) under its Faculty of Health Sciences
WHC provides Faculty with a legal framework within which to operate the research and other activities necessary to support its academic objectives
In addition WHC offers a range of products and services to Academics
Main purpose of the job:
To provide high-quality clinical care and conduct protocol-specifiedprocedures for trial participants ensuring participant safety accurate documentation and effective conduct of study visits in line with GCP
Location:
Edendale Lay Ecumencial Center Clinic Edendale Pietermaritzburg
Key performance areas: 1. Participant Clinical Care & Safety
Conduct all study-related clinical procedures in accordance with the protocol SOPs and GCP
Perform participant assessments including medical history symptom screening vitals pregnancy testing and targeted physical exams where delegated
Monitor participant safety identify and manage adverse events and escalate concerns to the Research Clinician/PI as required
2. Study Visit Implementation
Prepare for and conduct participant study visits (screening enrolment follow-up safety visits) according to protocol timelines
Ensure informed consent/assent is obtained and documented correctly for all participants (and caregivers where applicable)
3. Specimen Collection & Laboratory Procedures
Collect biological specimens (e.g. blood swabs urine) per protocol and GCP standards
Maintain correct specimen handling processing labelling chain-of-custody and timely delivery to the laboratory
Ensure accurate documentation in laboratory logs and shipping forms
4. Data Quality & Documentation
Complete all source documents CRFs and electronic data entries (MACRO/REDCap or other EDC platforms) accurately and in real time
Maintain organised participant files and study documentation (digital and hard-copy) in accordance with sponsor and WHC requirements
Respond to and resolve data queries in collaboration with data management teams
5. Communication & Team Collaboration
Maintain professional supportive interactions with participants to promote retention safety and adherence
Communicate clinical management issues and participant safety concerns promptly to the Study Coordinator and Principal Investigator
Attend regular study meetings trainings and debriefs
Support onboarding and mentoring of junior or newly assigned trial staff where relevant
Required minimum education and training:
Diploma in Nursing or Bachelors Degree in Nursing required
Qualified as a Professional Nurse
Fluent in English and Isi-Zulu
HIV Management and counselling course will be advantageous
Human Subjection Protection Certificate will be advantageous
TRREE (Training and Resources in Research Ethics Evaluation) will be advantageous
Good Clinical Practice Certificate will be an advantageous
Experience with Electronic data systems (e.g RedCap) and Excel will be advantageous
Knowledge of ALCOA Principles
Knowledge of Informed Consent Process
Drivers licence and able to drive manual vehicle
Professional Body Registration:
Registered with the South African Nursing Council (SANC) as a Professional Nurse
Required minimum work experience:
Minimum 2 - 3 years experience in a clinical or research environment
Experience in a research environment will be advantageous
Experience in NIMART or ART clinic will be advantageous
Ability to draw and process blood samples
Desirable additional education work experience and personal abilities:
Ability to lead and work independently as well as be part of a multidisciplinary team
A friendly informal attitude with excellent people skills
Ability to speak in local languages
Ability to work well under pressure
Ability to adapt to changing environment within the project needs
TO APPLY:
Only if you meet the minimum job requirements and experience as mentioned above you may submit a detailed updated CV
Please Apply Online and complete your registration via our website to enable and protect you as a candidate and to accept the new POPIA terms and conditions
This will then create your permanent profile with which you can apply for all jobs as advertised by AJ PERSONNEL
However you may remove your profile from AJ PERSONNEL when you are no longer in the job market
Please take note that the applicants who do not adhere to the above criteria will not be considered for the respective position
Wits Health Consortium will only respond to shortlisted candidates
Candidates who have not been contacted within two weeks of the closing date can consider their applications to be unsuccessful
Closing date:22 December 2025
Note: No CV will be accepted after the closing date
Please note:
WHC in accordance with its Employment Equity goals and plan will give preference to suitable applicants from designated groups as defined in the Employment Equity Act 55 of 1998 and subsequent amendments thereto
AJ Personnel is only responsible for advertising and the response handling on behalf of their client Wits Health Consortium
AJ Personnel does not have any salary or other information regarding the position
Background:Wits Health Consortium (Pty) Limited (WHC) is a wholly-owned Company of the University of the Witwatersrand Johannesburg (South Africa) under its Faculty of Health SciencesWHC provides Faculty with a legal framework within which to operate the research and other activities necessary to su...
Background:
Wits Health Consortium (Pty) Limited (WHC) is a wholly-owned Company of the University of the Witwatersrand Johannesburg (South Africa) under its Faculty of Health Sciences
WHC provides Faculty with a legal framework within which to operate the research and other activities necessary to support its academic objectives
In addition WHC offers a range of products and services to Academics
Main purpose of the job:
To provide high-quality clinical care and conduct protocol-specifiedprocedures for trial participants ensuring participant safety accurate documentation and effective conduct of study visits in line with GCP
Location:
Edendale Lay Ecumencial Center Clinic Edendale Pietermaritzburg
Key performance areas: 1. Participant Clinical Care & Safety
Conduct all study-related clinical procedures in accordance with the protocol SOPs and GCP
Perform participant assessments including medical history symptom screening vitals pregnancy testing and targeted physical exams where delegated
Monitor participant safety identify and manage adverse events and escalate concerns to the Research Clinician/PI as required
2. Study Visit Implementation
Prepare for and conduct participant study visits (screening enrolment follow-up safety visits) according to protocol timelines
Ensure informed consent/assent is obtained and documented correctly for all participants (and caregivers where applicable)
3. Specimen Collection & Laboratory Procedures
Collect biological specimens (e.g. blood swabs urine) per protocol and GCP standards
Maintain correct specimen handling processing labelling chain-of-custody and timely delivery to the laboratory
Ensure accurate documentation in laboratory logs and shipping forms
4. Data Quality & Documentation
Complete all source documents CRFs and electronic data entries (MACRO/REDCap or other EDC platforms) accurately and in real time
Maintain organised participant files and study documentation (digital and hard-copy) in accordance with sponsor and WHC requirements
Respond to and resolve data queries in collaboration with data management teams
5. Communication & Team Collaboration
Maintain professional supportive interactions with participants to promote retention safety and adherence
Communicate clinical management issues and participant safety concerns promptly to the Study Coordinator and Principal Investigator
Attend regular study meetings trainings and debriefs
Support onboarding and mentoring of junior or newly assigned trial staff where relevant
Required minimum education and training:
Diploma in Nursing or Bachelors Degree in Nursing required
Qualified as a Professional Nurse
Fluent in English and Isi-Zulu
HIV Management and counselling course will be advantageous
Human Subjection Protection Certificate will be advantageous
TRREE (Training and Resources in Research Ethics Evaluation) will be advantageous
Good Clinical Practice Certificate will be an advantageous
Experience with Electronic data systems (e.g RedCap) and Excel will be advantageous
Knowledge of ALCOA Principles
Knowledge of Informed Consent Process
Drivers licence and able to drive manual vehicle
Professional Body Registration:
Registered with the South African Nursing Council (SANC) as a Professional Nurse
Required minimum work experience:
Minimum 2 - 3 years experience in a clinical or research environment
Experience in a research environment will be advantageous
Experience in NIMART or ART clinic will be advantageous
Ability to draw and process blood samples
Desirable additional education work experience and personal abilities:
Ability to lead and work independently as well as be part of a multidisciplinary team
A friendly informal attitude with excellent people skills
Ability to speak in local languages
Ability to work well under pressure
Ability to adapt to changing environment within the project needs
TO APPLY:
Only if you meet the minimum job requirements and experience as mentioned above you may submit a detailed updated CV
Please Apply Online and complete your registration via our website to enable and protect you as a candidate and to accept the new POPIA terms and conditions
This will then create your permanent profile with which you can apply for all jobs as advertised by AJ PERSONNEL
However you may remove your profile from AJ PERSONNEL when you are no longer in the job market
Please take note that the applicants who do not adhere to the above criteria will not be considered for the respective position
Wits Health Consortium will only respond to shortlisted candidates
Candidates who have not been contacted within two weeks of the closing date can consider their applications to be unsuccessful
Closing date:22 December 2025
Note: No CV will be accepted after the closing date
Please note:
WHC in accordance with its Employment Equity goals and plan will give preference to suitable applicants from designated groups as defined in the Employment Equity Act 55 of 1998 and subsequent amendments thereto
AJ Personnel is only responsible for advertising and the response handling on behalf of their client Wits Health Consortium
AJ Personnel does not have any salary or other information regarding the position
AJ Personnel offers expert recruitment services and job vacancies across South Africa. Trusted among top recruitment agencies for connecting talent with opportunity.