Assist with the review and revision of standard operating procedures per study-specific needs as needed Practice (GCP), Protocol requirements, Standard Operating Procedures (SOPs), and Regulatory Essential Documents within a clinical research environment in Quality Control and Quality Assurance Desirable additional education
the study protocol, and the site's standard operating procedures Location: 22 Esselen Street, Hillbrow Johannesburg Key performance areas: Oversee all operations in the clinical trial to ensure protocol and Importance as per protocol requirements. Quality control of patient files and data entries (i.e., eCRF's
Assist with the review and revision of standard operating procedures per study-specific needs as needed Practice (GCP), Protocol requirements, Standard Operating Procedures (SOPs), and Regulatory Essential Documents within a clinical research environment in Quality Control and Quality Assurance Desirable additional education
the study protocol, and the site's standard operating procedures Location: 22 Esselen Street, Hillbrow Johannesburg Key performance areas: Oversee all operations in the clinical trial to ensure protocol and Importance as per protocol requirements. Quality control of patient files and data entries (i.e., eCRF's
Faculty with a legal framework within which to operate the research and other activities necessary to scheduling disciplinary inquiries, grievances, and operational requirements Provide advice and facilitation
Faculty with a legal framework within which to operate the research and other activities necessary to scheduling disciplinary inquiries, grievances, and operational requirements Provide advice and facilitation
project files and filling system Support the quality control of patient files and data entries (i.e., eCRF's
project files and filling system Support the quality control of patient files and data entries (i.e., eCRF's
reports and feedback on all activities Quality control CRFs and other study documents Safekeeping of project
reports and feedback on all activities Quality control CRFs and other study documents Safekeeping of project