of study visits, follow up of participants, data entry, and progress report for ongoing projects S/he will and resolve queries that are generated by data management staff Assist with scheduling study visits and Good problem-solving skills Good organizational, management, and communications skills Good computer literacy
of study visits, follow up of participants, data entry, and progress report for ongoing projects S/he will and resolve queries that are generated by data management staff Assist with scheduling study visits and Good problem-solving skills Good organizational, management, and communications skills Good computer literacy
as per study requirements/SOPs
sources as per study requirements/SOPs Collect, manage and maintain quality data for research and operations documentation in accordance with SOPs Support data entry as needed Facilitate reimbursement for study participation accountability for tasks and demonstrates effective self-management Follow through to ensure that quality and productivity
sources as per study requirements/SOPs Collect, manage and maintain quality data for research and operations documentation in accordance with SOPs Support data entry as needed Facilitate reimbursement for study participation accountability for tasks and demonstrates effective self-management Follow through to ensure that quality and productivity
an appropriate PV, vigilance system, and Risk Management to ensure appropriate oversight for products responsibilities. Ensure the pro-active Benefit Risk Management throughout product life cycle translating global 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 Impact assessments and action as required on a local level Provide content to the Pharmacovigilance System
an appropriate PV, vigilance system, and Risk Management to ensure appropriate oversight for products responsibilities. Ensure the pro-active Benefit Risk Management throughout product life cycle translating global 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 Impact assessments and action as required on a local level Provide content to the Pharmacovigilance System
risk & environmental-related topics (noise levels, use of machinery, spillages, Health, security and coach where applicable.
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 risk registers Communicate risk control and risk management information by analyzing data, developing indictors and presenting required reports and advising management accordingly. Liaise with external bodies eg. produce and present required reports to advise management accordingly. Engage with external bodies (eg
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 risk registers Communicate risk control and risk management information by analyzing data, developing indictors and presenting required reports and advising management accordingly. Liaise with external bodies eg. produce and present required reports to advise management accordingly. Engage with external bodies (eg