the study protocol, and the site's standard operating procedures
Location:
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 Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants events Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator
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 Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants events Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator
improve and maintain essential IT operations, including operating systems, security tools, applications in place is functional as well as staff and operational requirements are met
finance and procurement policies
relevant finance and procurement policies Analyse data to track progress towards targets and optimize implementation management of multiple stakeholders Experience in data analysis and utilization Good understanding of quality reporting requirements Knowledge of clinical and data management and analysis Proactive, energetic team
relevant finance and procurement policies Analyse data to track progress towards targets and optimize implementation management of multiple stakeholders Experience in data analysis and utilization Good understanding of quality reporting requirements Knowledge of clinical and data management and analysis Proactive, energetic team