inspections, errors and corrective action. Analyse quality data and generate reports for management. Ensure that received. Develop and / or update procedurs for capture, investigation and documentation of product complaints
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
the Medical Industry {Preferable} Experience with data collection and trending Experience with Quality NRCS, ICASA (Preferred) KPI DATA COLLECTION AND ANALYTICS Ensure data is provided as per approved KPI Metrics for sections under responsibility Perform data analysis and trending remarks MEDICAL DEVICE FILE product dashboards and supporting documents. Trend KPI data and provide report timeously for Management Review timelines for reporting is adhered to. Trend KPI data and provide report timeously for Management Review
the Medical Industry {Preferable} Experience with data collection and trending Experience with Quality NRCS, ICASA (Preferred) KPI DATA COLLECTION AND ANALYTICS Ensure data is provided as per approved KPI Metrics for sections under responsibility Perform data analysis and trending remarks MEDICAL DEVICE FILE product dashboards and supporting documents. Trend KPI data and provide report timeously for Management Review timelines for reporting is adhered to. Trend KPI data and provide report timeously for Management Review
calibrated and functioning correctly. Record and analyze data, documenting results accurately in laboratory notebooks including those related to patient confidentiality and data integrity. Education and/or Work Experience Requirements: management systems (LIMS) and other computerized data management systems. Knowledge of laboratory safety
calibrated and functioning correctly. Record and analyze data, documenting results accurately in laboratory notebooks including those related to patient confidentiality and data integrity. Education and/or Work Experience Requirements: management systems (LIMS) and other computerized data management systems. Knowledge of laboratory safety
programs to gather data on air, water, soil, and biodiversity. Analyse environmental data using advanced
programs to gather data on air, water, soil, and biodiversity. Analyse environmental data using advanced
products Conduct dossier due diligence to ensure all data gaps are addressed Work in collaboration with internal