Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality of the relevant studies and SOPs, knowledge of clinical research documentation Computer literate with
Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality of the relevant studies and SOPs, knowledge of clinical research documentation Computer literate with
technique. Conduct all work according to Good Clinical Laboratory Practice (GCLP) guidelines and auditable-
technique. Conduct all work according to Good Clinical Laboratory Practice (GCLP) guidelines and auditable-
Responsible to manage and maintain the onsite medical clinic and facility, equipment and medical consumable including calibration of alcohol breathalyzer, all clinic equipment and health and safety department equipment records and the safekeeping thereof in the onsite clinic Handling all Department of Employment and Labour
Responsible to manage and maintain the onsite medical clinic and facility, equipment and medical consumable including calibration of alcohol breathalyzer, all clinic equipment and health and safety department equipment records and the safekeeping thereof in the onsite clinic Handling all Department of Employment and Labour
Gauteng Province with just over 300 students enrolled in Grades 8 -12. Grade 12. Students write the
Gauteng Province with just over 300 students enrolled in Grades 8 -12. Grade 12. Students write the
safety of their employees. Using their in-house clinical health expertise, data analytics, statistical
Participating in the development or implementation of clinical trial protocols to meet regulatory requirements