throughout product life cycle translating global safety data to insights and actions tailoring to local specificities Seychelle, Cape Verde) Main responsibilities: Local Medical Safety Responsibility & Benefit Risk Management: the local Medical and Marketing organization in collaboration with the International Medical Safety leader Aggregate reports: Work with LSO/CSTL to provide medical input and insights for aggregate reports while regulations (for drugs non-medicinal products & Medical Devices in the scope of responsibilities), evaluation
throughout product life cycle translating global safety data to insights and actions tailoring to local specificities Seychelle, Cape Verde) Main responsibilities: Local Medical Safety Responsibility & Benefit Risk Management: the local Medical and Marketing organization in collaboration with the International Medical Safety leader Aggregate reports: Work with LSO/CSTL to provide medical input and insights for aggregate reports while regulations (for drugs non-medicinal products & Medical Devices in the scope of responsibilities), evaluation
and selectively record anatomical images, physical data and real time physiological information for health and work in conjunction with other medical practitioners for medical diagnosis as appropriate Location: and generate reports, capturing data and images into an electronic data capture system Must be able to project goals on time and on budget Work with medical professionals to develop standard operating procedures
and selectively record anatomical images, physical data and real time physiological information for health and work in conjunction with other medical practitioners for medical diagnosis as appropriate Location: and generate reports, capturing data and images into an electronic data capture system Must be able to project goals on time and on budget Work with medical professionals to develop standard operating procedures
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
conduct analysis of data, and publish scientific articles Enhance routine programme data analytics to inform team and other relevant staff Supervise fieldwork (data collection, interviews, etc.) Screen participants Extract data from participant medical records Conduct data collection and data quality processes Data management Storage and archiving of data according to SOP's (electronic and hard copy data) Adherence to study protocols reporting requirements Conduct data analysis according to agreed data analysis plan and write up results
conduct analysis of data, and publish scientific articles Enhance routine programme data analytics to inform team and other relevant staff Supervise fieldwork (data collection, interviews, etc.) Screen participants Extract data from participant medical records Conduct data collection and data quality processes Data management Storage and archiving of data according to SOP's (electronic and hard copy data) Adherence to study protocols reporting requirements Conduct data analysis according to agreed data analysis plan and write up results
study participants, conducting requisite sample and data collection as per protocol and Standard Operating documentation/questionnaires and checklists