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Clinical Data Monitor Jobs in South Africa

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Temperature Monitor - Port Elizabeth Market Related Market Related

 Phakisa Holdings LtdPort Elizabeth

Phakisa Holdings are looking for a Temperature Monitor in Port Elizabeth Market Related Role Overview Responsibility : A Temperature Monitor is primarily responsible for continuously monitoring and recording temperatures safety of perishable goods. Key Responsibilities: Monitoring : Regularly check and record temperatures in Use of temperature monitoring devices and systems, including digital thermometers, data loggers, and automated automated monitoring systems. Reporting : Generate and maintain logs or reports of temperature readings


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Fieldworkers (x 4 Three Months Fixed Term Contract Mthatha Wits Rhi)

Mthatha

will be responsible for participant recruitment and data collection at the allocated study sites

  • Where appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice
  • Conduct Informed Consent discussion schedule
  • Conduct data extraction from clinic registers, patient records or other relevant data sources as per and maintain quality data for research and operations purposes.
  • Capture data into study databases


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  • Fieldworkers (x4 Three Months Fixed Term Contract Tshwane Wits Rhi)

    Pretoria

    will be responsible for participant recruitment and data collection at the allocated study sites

  • Where appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice
  • Conduct Informed Consent discussion schedule
  • Conduct data extraction from clinic registers, patient records or other relevant data sources as per and maintain quality data for research and operations purposes.
  • Capture data into study databases


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  • Fieldworkers (x2 Three Months Fixed Term Contract Hillbrow Wits Rhi)

    Hillbrow

    will be responsible for participant recruitment and data collection at the allocated study sites

  • Where appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice
  • Conduct Informed Consent discussion schedule
  • Conduct data extraction from clinic registers, patient records or other relevant data sources as per and maintain quality data for research and operations purposes.
  • Capture data into study databases


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  • Fieldworker Hillbrow, South Africa

     Aj PersonnelHillbrow

    will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e


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    Fieldworker Pretoria, South Africa

     Aj PersonnelSouth Africa

    will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e


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    Fieldworkers (x 4 Three Months Fixed Term Contract Mthatha Wits Rhi)

     Aj PersonnelSouth Africa

    will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e


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    Fieldworkers (x2 Three Months Fixed Term Contract Hillbrow Wits Rhi)

     Aj PersonnelHillbrow

    will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e


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    Fieldworker Mthatha, South Africa

     Aj PersonnelSouth Africa

    will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e


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    Fieldworkers (x4 Three Months Fixed Term Contract Tshwane Wits Rhi)

     Aj PersonnelSouth Africa

    will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate appropriate, they will also contribute towards ongoing monitoring and administration of the designated studies; participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e


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