About the position
Background:
- The Wits Reproductive Health and HIV Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa’s health challenges
- It is located within the University of the Witwatersrand and addresses some of the greatest public health concerns affecting our region, including HIV and its related problems, sexual and reproductive health, and vaccinology
Main purpose of the job:
- To monitor and ensure compliance with regulatory and good clinical research practice requirements within research studies within Clinical Research Centre
Location:
- 7 Esselen Street, Hillbrow, Wits RHI Research Centre Clinical Research Site (CRS)
Key performance areas:
- Prepare applications and submissions to IRB’s, SAHPRA, DOH, NHRD as needed
- Create, establish and maintain regulatory systems for Wits RHI studies per SAHPRA, HREC, sponsor and DOH requirements. Print and file regulatory documentation
- Work with the Regulatory Oversight Group (ROG) and Research Review Committee (RRC) as needed and provide expert guidance on the requirements of local and international regulatory bodies and frameworks and support the department to comply with those requirements
- Track annual recertification submissions to HREC
- Review systems and recommend improvements to streamline the creation and maintenance of trial documentation and review and advise on improvements and standardisation of quality control and assurance systems with respect to improved compliance with regulatory frameworks
- Actively participate in the submission of research protocols and where appropriate assist in writing funding proposals for improvements of monitoring, evaluation and quality control of data
- Ensure site delegation logs are updated when there are staffing changes
- Ensure adequate training completed by staff members and training logs completed
- Ensure staff adhere to responsibilities defined in site delegation logs per qualifications and training
- Ensure that all SOPs have been read and signed by all staff
- When SOPs revised circulate new signage sheets for completion on review
- Prepare site informed consent forms and prepare, review and revise standard operating procedures per study specific needs
- Review and ensure that the study has all essential regulatory documentation
- Assist sponsors / monitors before, during and after the review
- Perform duties per study Delegation of Authority Logs
- Ensure participants are enrolled per defined eligibility criteria
- Provide training to staff in areas of expertise to reduce repetitive errors noted during study file review
- Assist in completion of corrective action for both internal and external monitoring reviews
- Ensure site is well prepared for internal and external lab, pharmacy, clinical, social science and community monitoring reviews
- Ensure documentation is adequate on study specific procedures
- Assess compliance to Good Clinical Practice (GCP), Standard Operating Procedures (SOPs) and Regulatory Essential Documents per sponsor requirements and to determine the accuracy of research records
- Take ownership and accountability for tasks and demonstrates effective self-management
- Follow through to ensure that quality and productivity standards of own work are consistently and accurately maintained
- Maintain a positive attitude and respond openly to feedback
- Take ownership for driving own career development by participating in ongoing training and development activities such as conferences, workshops etc
Required minimum education and training:
- 3 year Degree in a Health related field
Required minimum work experience:
- Minimum 1-3 years relevant work experience within a clinical research environment in regulatory compliance
Desirable additional education, work experience and personal abilities:
- A post graduate degree in Quality Management would be an added advantage
- Understanding of the research language, detailed knowledge and understanding of the relevant studies and SOP’s, knowledge of clinical research documentation
- Detailed knowledge of regulatory application and approval processes
- Computer literate with ability to create or work with databases
- Fluent in English, fluency in one of the other official SA languages particularly Zulu or Sesotho would be an added advantage
- Good written and verbal communication skills
- Strategic thinking and problem-solving skills
- Conscientious and precise delivery of work even when under pressure
- Effective self-management, resourcefulness and initiative to solve problems
- Excellent communication and presentation skills
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 April 2026
- 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
Desired Skills:
- Research
- Regulatory Compliance
- SOP
- Computer Literacy
- Communication Skills
- Self Management
