focused on the clinical and molecular epidemiology of vaccine-preventable disease, clinical development coordinating all aspects of clinical research study activities and ensuring that clinical research projects are including paper logs and electronic logs Oversee management and printing of up-to-date versions of study attend the 1-year, 2-year, and 3-year face-to-face clinical visit Maintain logs to remind study staff of the neurodevelopmental assessment Oversee relevant study stock management and ensure adequate stock levels are always maintained
focused on the clinical and molecular epidemiology of vaccine-preventable disease, clinical development coordinating all aspects of clinical research study activities and ensuring that clinical research projects are including paper logs and electronic logs Oversee management and printing of up-to-date versions of study attend the 1-year, 2-year, and 3-year face-to-face clinical visit Maintain logs to remind study staff of the neurodevelopmental assessment Oversee relevant study stock management and ensure adequate stock levels are always maintained
over 5000 clients Reporting to Regulatory Affairs Manager Job purpose: Support the Regulatory team to provide external Partners and Principals, and to control and manage a portfolio of product outputs. To ensure legal processing of regulatory applications. Key Job Outputs Manage work streams for- and report on the assigned portfolio devices. Conduct dossier due diligence to ensure all data gaps are addressed, in preparation for dossier call activities. Quality Management System: Comply with all requirements of Quality Management System to ensure
Environmental Officer in support to the Environmental Manager is responsible for the coordination,
administration
coaching to successfully manage the ISO14001:2015 Environmental Management system for
both manufacturing
licensing. Communicate to Environmental Manager
responsibility. • Assist in maintaining the Quality Management system. • Perform admin duties. • Assist in maintaining