CRS’s data
Location:
Ward21 CRS's data Performing data cleaning, collaborating with the data manager to enhance data collection preparing data for analysis and use Monitor project progress and key trends in performance and data quality performance areas: Contribute to the development of a data quality strategy that aligns with the Ward21 CRS's appropriate data analysis and reporting Set up and implement systems for monitoring compliance with data quality determine data quality and integrity Assess system performance and design, as well as its effect on data quality
Ward21 CRS's data Performing data cleaning, collaborating with the data manager to enhance data collection preparing data for analysis and use Monitor project progress and key trends in performance and data quality performance areas: Contribute to the development of a data quality strategy that aligns with the Ward21 CRS's appropriate data analysis and reporting Set up and implement systems for monitoring compliance with data quality determine data quality and integrity Assess system performance and design, as well as its effect on data quality
projections and planning
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
Maintain high communication standards. Utilize data analytics for audit planning. Review and approve Prepare proper working papers and documentation. Use data analytics to support fieldwork and testing. Prioritize
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
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
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