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Medi Clinic Nursing Auxiliary Vacancies Jobs in Johannesburg, Gauteng

Jobs 1-4 of 4
  •  Scientific / QA
  •  Aj Personnel

Research Medical Officer (doctor Mycology 12 Months Fixed Term Contract)

 Aj PersonnelSoweto

epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials brings together leading academic researchers, clinical and public health leaders, non-governmental organisations Main purpose of the job: To join the sub-EFFECT clinical study site(s) team and manage day-to-day activities Rossmore NICD, Sandringham Key performance areas: Clinical study management Contribute to the development requirements Participate in regular meetings between the clinical teams and cover duties of the EFFECT trial study


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Research Doctor Soweto, South Africa

 Aj PersonnelSoweto

epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials brings together leading academic researchers, clinical and public health leaders, non-governmental organisations Main purpose of the job: To join the sub-EFFECT clinical study site(s) team and manage day-to-day activities Rossmore NICD, Sandringham Key performance areas: Clinical study management Contribute to the development requirements Participate in regular meetings between the clinical teams and cover duties of the EFFECT trial study


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Project Manager Hillbrow, South Africa

 Aj PersonnelHillbrow

responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education


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Project Managers (x2 Wits Rhi) From To (basic Plus Benefits) - Yearly

 Aj PersonnelHillbrow

responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education


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