accurate mapping of clinical trial data into a harmonised database, support data acquisition processes, apply notifications, and assist senior staff in improving the data harmonisation platform from a clinical standpoi study
samples etc.) ensuring availability of records for data and root cause analysis. Inform the relevant persons organise data, analyse information and make recommendations. Ability to input data into data capturing software
supervisors, pharmacist or manufacturing manager. Capturing of daily production activities, to facilitate
monitoring of animal species. The data will primarily be acoustic data, however additional sources may review, software and model implementation, data analysis, data annotation, writing manuscripts, and giving
monitoring of animal species. The data will primarily be acoustic data, however additional sources may review, software and model implementation, data analysis, data annotation, writing manuscripts, and giving
accidents. Document and report incidents, analyze data, and recommend corrective actions. Maintaining safety
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
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
equipment and facilities. Test product and record data concerning materials and product according to the
hands-on performance of protocol requirements, data analysis and final report writing. Provide detailed