refine data collection tools, design, develop, and maintain databases, perform logic-based data validation validation rules for quality assurance on data, timely reporting, and documentation Location: VIDA – Chris Johannesburg, Gauteng Key performance areas: Technical Data Management and Analytics Contribute to refining development of HDSS data collection forms Draw up the specifications for harmonized data sets to send out participating HDSS sites Guide and lead routine data operational reports to inform on smooth field processes
refine data collection tools, design, develop, and maintain databases, perform logic-based data validation validation rules for quality assurance on data, timely reporting, and documentation Location: VIDA – Chris Johannesburg, Gauteng Key performance areas: Technical Data Management and Analytics Contribute to refining development of HDSS data collection forms Draw up the specifications for harmonized data sets to send out participating HDSS sites Guide and lead routine data operational reports to inform on smooth field processes
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants 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
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants 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
Main purpose of the job: To provide best practice data collection, clinical assessments, collection of update study-specific job aides Collect participant data from medical notes and complete CRFs Maintain full protocol and SOPs Prepare all relevant reports Capture data timeously and accurately Provide regular updates
Main purpose of the job: To provide best practice data collection, clinical assessments, collection of update study-specific job aides Collect participant data from medical notes and complete CRFs Maintain full protocol and SOPs Prepare all relevant reports Capture data timeously and accurately Provide regular updates
standards. Approving, maintaining, and accurately capturing and authorizing any changes to manufacturing master re-occurrence of incidents. Ensuring all necessary data, training of personnel and applicators, and health
visit projections and planning Review data to identify trends, data quality issues, and areas for improvement patient files and data entries (i.e., eCRF's, CRF's) Support the storage and archiving of data as per the SOP visits, audits, site inspections, and similar Support data clean-up activities resulting from assessments Ensure
visit projections and planning Review data to identify trends, data quality issues, and areas for improvement patient files and data entries (i.e., eCRF's, CRF's) Support the storage and archiving of data as per the SOP visits, audits, site inspections, and similar Support data clean-up activities resulting from assessments Ensure
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