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
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