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  • Posted: Mar 16, 2023
    Deadline: Not specified
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    The South African Medical Research Council (SAMRC) was established in 1969 with the aim to deliver on a mandate to promote the improvement of the health and the quality of life of the population of our country through research, development and technology transfer. The scope of the SAMRC’s research includes basic laboratory investigations, clinical rese...
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    Project Coordinator - Study Coordinator - HIDRU - R 598A

    PROJECT CO-ORDINATOR: STUDY CO-ORDINATOR

    • Duration: One-Year Contract
    • The SAMRC’s HIV and Other Infectious Diseases Research Unit (HIDRU) seeks to appoint an experienced and competent Study Co-ordinator to fulfill the following responsibilities:

    Responsibilities:

    • Co-ordinate research activities related to the implementation of multiple research protocols at clinical research site
    • Ensure optimum clinic flow to facilitate effective conduct of multiple clinical research studies
    • Monitor and supervise quality control of all study data and informed consent procedures
    • Ensure that corrective and preventative action for citations are generated from internal/external audits
    • Ensure that Standard Operating Procedures (SOP’s) are updated, implemented and monitored
    • Supervise data collection and associated document management
    • Monitor and supervise the recruitment and retention efforts at the clinical research site
    • Manage and supervise a multidisciplinary research team
    • Manage participant reimbursement and financial advances
    • Supervise operational activities at sites
    • Assist with scientific report writing/publications and presentations.

    Core Requirements:

    • Honours Degree in the Biomedical or Social Science environment or similar relevant qualification or higher
    • 4 years’ experience in the HIV/Health research environment
    • 2 years’ experience with training and supervision
    • 2 years’ coordination and management experience.
    • Computer literate in MS packages and spreadsheets

    Advantageous:

    A Master’s degree

    • Understanding of Good Clinical Practice or a valid certificate in Good Clinical Practice
    • Applicant must be able to work under pressure and multi-task
    • Effective interpersonal skills
    • Experience with electronic data capture (EDC)

    Method of Application

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