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  • Posted: Jul 8, 2026
    Deadline: Jul 17, 2026
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  • The Desmond Tutu Health Foundation, housed within the Desmond Tutu HIV Centre (DTHC) at the University of Cape Town, is committed to the pursuit of excellence in research, treatment, training and prevention of HIV and related infections in Southern Africa. Fully self- funded by grants and other investigator raised funds, our shared vision for the future inc...
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    Data Manager

    Requirements

    • Undergraduate degree in medical, scientific, biological, statistical, computer science, or related field
    • At least 2 years of experience in managing databases within a research environment
    • At least 2 year’s demonstrable experience building and managing complex data collection tools using Redcap (please detail in cover letter)
    • At least 1 year of supervisory and staff management
    • Proficient in MS Excel and Access and be able to design a database, run and resolve data queries
    • Good Clinical Practice (GCP) certificate
    • Valid code 8 driver’s license

    Advantageous:

    • Experience with statistical packages e.g. STATA, SPSS, SAS or R
    • Knowledge of HIV & ART

    Responsibilities:

    Research Data Management:

    • Institutionalize high-quality data collection, management, and quality assurance systems and processes for current studies and ARV databases using REDCap and other platforms.
    • Develop and implement real-time data quality assurance processes and procedures
    • Perform data cleaning and log data queries for investigation
    • Support the design of compatible and integrated systems for data coordination and sharing with research partners
    • Work with study Project lead and Project Manager to develop data management and quality assurance plans, including project progress monitoring tools
    • Develop and automate statistical dashboards on project implementation and key study variables
    • Prepare and extract analytic datasets, and perform analyses for PI, project lead and managers 

    System Design and Maintenance:

    • Provide oversight for collection of data from the studies, including:
    • Incorporating data from database or data system,
    • Supervise the organization, cleaning, and verifying complete data entry by research assistants and fieldworkers;
    • Prepare data for use in analyses by overseas and South African-based investigators.
    • Oversee all QC and QA processes
    • Ensure that data is collected and QCed as per the Quality management plan

    Staff Management:

    • Manage staff and oversee their work.
    • Manage the quality of databases and supervise data-entry staff
    • Ensure training of and optimal implementation of all components of project data management
    • Train and support field-based data collection staff members
    • Attend project management meetings

    go to method of application »

    Retention Officer

    Requirements

    • Grade 12 certificate
    • At least 2 years’ experience in participant retention, follow-up, adherence support, or community-based health programmes.
    • Experience in participant tracing, follow-up, or lost-to-follow-up (LTFU) management
    • Knowledge of HIV/AIDS, adolescent sexual health, PrEP
    • Experience in Addressing barriers to participation by coordinating logistical support (e.g., transport assistance, flexible appointment scheduling and appointment reminders)
    • Experience with Data and Compliance: Track participant retention rates, draft protocol-specific retention Standard Operating Procedures (SOPs and compile routine reports on attrition
    • Intermediate computer skills (MS Word, Excel, PowerPoint)
    • Fluency in English and/or Afrikaans and/or IsiXhosa
    • Ability to take initiative
    • Attention to detail
    • Ability to work with teams and independently
    • Good planning and organising
    • Time management

    Advantageous:

    • Experience in a community-based research projects
    • Valid Driver’s license
    • Good Clinical Practice (GCP) Certificate
    • Training in PrEP (including lenacapavir)

    Responsibilities:

    Participant Retention & Follow-up

    • Maintain regular communication with participants and address any concerns or challenges
    • Conduct follow-up activities, including telephonic follow-ups and home visits
    • Track participant appointments and proactively follow up on missed visits
    • Develop and implement retention plans to enhance participant engagement and minimise loss to follow-up

     Participant Engagement & Support

    • Support participant counselling activities and provide basic adherence support
    • Facilitate youth reference group (YRG) and/or intervention sessions in alignment with project objectives
    • Support participant engagement initiatives to strengthen retention and study participation

     Study Coordination & Support

    • Support the research team with study-specific activities, including focus group discussions, consent form quality control, and participant follow-up
    • Collaborate with the research team to support recruitment strategies aligned with study objectives
    • Support recruitment activities on mobile clinics and assist with community-based surveys

     Data Management & Reporting

    • Maintain accurate and up-to-date records of recruitment and retention activities
    • Develop and manage retention tracking tools, including weekly and monthly PrEP retention reports
    • Provide regular activity updates and progress reports to the project team
    • Follow up on HIV self-test results and capture data accurately in REDCap
    • Conduct informed consent form (ICF) quality checks and report findings to the Project Manager.

    Operational & Clinical Support

    • Work closely with clinical staff to support PrEP and STI treatment packaging and distribution
    • Coordinate PrEP courier services and liaise with the Data team regarding scheduled deliveries

    Administrative & Compliance

    • Assist with filing and maintaining research documentation and participant records
    • Ensure strict adherence to confidentiality and ethical research standards
    • Perform any other project-related duties as required

    Method of Application

    Use the link(s) below to apply on company website.

     

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