job:
the job: To oversee the collection of interview data and biological specimens according to best practices update study-specific job aides Collect participant data from medical notes and complete CRFs Maintain full SOPs Prepare health facilities and communities for data study entry Provide regular updates on the study
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
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
Information on product labels and product technical data sheets. Liaise with "Toll manufacturing" customers Management To build and maintain product formulation data base (spread sheet with hyperlink references) Background function To build an approved, supplier/ ingredient data base To Create Procedures and Works Instructions
job:
edge of data quality assurance and control (QA/QC) processes
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