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 participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per Collect, manage and maintain quality data for research and operations purposes. Capture data into study Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per Collect, manage and maintain quality data for research and operations purposes. Capture data into study Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
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 experience working in midwifery or with ante-natal clinics or programmes Good understanding of issues and
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 experience working in midwifery or with ante-natal clinics or programmes Good understanding of issues and
development, implementation and management of a standardized integrated SHERQ management system as per the required ensure quality control and compliance. Provide management and staff training Ensure that all traceability Communicate risk control and risk management information by analyzing data, developing indictors, producing and presenting required reports and advising management accordingly. Liaise with external bodies eg. developments. Communication and Reporting Analyse data, develop leading indicators, determine trends and
development, implementation and management of a standardized integrated SHERQ management system as per the required ensure quality control and compliance. Provide management and staff training Ensure that all traceability Communicate risk control and risk management information by analyzing data, developing indictors, producing and presenting required reports and advising management accordingly. Liaise with external bodies eg. developments. Communication and Reporting Analyse data, develop leading indicators, determine trends and
an appropriate PV, vigilance system, and Risk Management to ensure appropriate oversight for products pro-active Benefit Risk Management throughout product life cycle translating global safety data to insights and Medical Safety Responsibility & Benefit Risk Management: Establish Product knowledge with a focus on of AE/PQC material, where needed. PV contract management: Support LSO/CSTL with the local Pharmacovigilance Pharmacovigilance System Master File (PSMF) contributions and data, as needed, accurately and in a timely manner. Responsible
an appropriate PV, vigilance system, and Risk Management to ensure appropriate oversight for products pro-active Benefit Risk Management throughout product life cycle translating global safety data to insights and Medical Safety Responsibility & Benefit Risk Management: Establish Product knowledge with a focus on of AE/PQC material, where needed. PV contract management: Support LSO/CSTL with the local Pharmacovigilance Pharmacovigilance System Master File (PSMF) contributions and data, as needed, accurately and in a timely manner. Responsible