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  • Posted: Apr 11, 2022
    Deadline: Not specified
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    Africa Health Research Institute’s vision is optimal health and well-being of under-resourced populations. Africa Health Research Institute (AHRI) is an independent, transdisciplinary scientific research institute based across two campuses in the province of KwaZulu-Natal (KZN) in South Africa. AHRI’s research combines population, basic and translational, social, and clinical sciences to understand and intervene in the health and well-being of South African communities. AHRI works in partnership with local communities and South African academic, governmental, and other policy stakeholders and collaborates with over 60 institutions globally. AHRI prioritizes the training of the next generation of African scientists.
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    Research Study Coordinator

    The incumbent will be based at the AHRI Durban campus but may be required to travel between AHRI-Durban campus and AHRI- Somkhele campus to provide oversight and monitoring of clinical research activities.

    Specification    

    • Participate in study team meetings as required and provide constructive feedback and support to other team members
    • Liaise with staff at research sites and where necessary at other clinical sites.
    • Quality control/Quality Assurance and data collection oversight
    • Ensure that corrective and preventative action is done timeously
    • Assist with site QC processes: Complete other QC checks as required.
    • Co-ordinate research activities related to the implementation of the multiple study protocols at the site
    • Site infrastructure supervision of teams and maintenance
    • Monitoring and supervision of informed consent procedures across studies
    • Ensuring documentation management and corrective action on internal/external monitoring reports
    • Developing study specific standard operating best practices for clinical study sites and ensure they meet all local and/ international regulations
    • Ensuring implementation, monitoring and updating Standard Operating Procedures, (SOPs) for all protocol procedures, as per GCP
    • Managing risk assessments to ensure that study participants and AHRI are protected, and risks are mitigated for studies conducted
    • Ensuring recruitment and retention efforts are optimized and amended as needed through study progression
    • Training and supervision of research teams and assisting Project Managers/Program Manager with setting and assessing key performance areas of staff
    • Assisting Project Managers/Program Manager with preparation and submission of documentation to Ethics and Regulatory authorities
    • Assisting with scientific report writing/publications and presentations
    • Compile reports to PIs, collaborators, sponsors and funders etc as needed
    • Assist with compiling of budgets when required
    • Supervision of participant re-imbursement & reconcile cash close-outs

    Requirements    

    Minimum Qualifications

    • Post Graduate qualification in a Health or Social Science discipline
    • Must possess a valid South African Code B Driver’s License and own vehicle

    Minimum Experience

    • Minimum of 3 years’ experience in clinical research setting of which 2 years’ experience must be coordinating research studies

    Cloisng Date: 24th, April 2022

    Method of Application

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