will be responsible for participant recruitment and data collection at the allocated study sites
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support Support translation and transcription of qualitative data if required Adhere to Good Clinical Practice Standards
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support Support translation and transcription of qualitative data if required Adhere to Good Clinical Practice Standards
and selectively record anatomical images, physical data and real time physiological information for health and generate reports, capturing data and images into an electronic data capture system Must be able to
and selectively record anatomical images, physical data and real time physiological information for health and generate reports, capturing data and images into an electronic data capture system Must be able to
study participants, conducting requisite sample and data collection as per protocol and Standard Operating documentation/questionnaires and checklists
study participants, conducting requisite sample and data collection as per protocol and Standard Operating documentation/questionnaires and checklists Ensure the data collected is complete and free from errors through abnormality in data collection to Study Coordinators or Medical Officers Collect required data from participant recruited daily in the study electronic database Address data queries and resolve them accordingly Any other duties
study participants, conducting requisite sample and data collection as per protocol and Standard Operating documentation/questionnaires and checklists Ensure the data collected is complete and free from errors through abnormality in data collection to Study Coordinators or Medical Officers Collect required data from participant recruited daily in the study electronic database Address data queries and resolve them accordingly Any other duties
job:
throughout product life cycle translating global safety data to insights and actions tailoring to local specificities Pharmacovigilance System Master File (PSMF) contributions and data, as needed, accurately and in a timely manner. Responsible language(s) and English language required Good in data analysis and reporting Proficiency in global and