A pharmaceutical company in Lombardia, Italy is seeking a Senior Associate in Global Regulatory Affairs Operations. The role involves leading regulatory data governance and managing xEVMPD data, ensuring compliance with EMA guidelines. The ideal candidate has a Master’s degree in a scientific discipline and hands-on experience with Veeva applications. This position is for a fixed-term contract covering maternity leave, making it a great opportunity for professionals looking to contribute to regulatory processes in the pharmaceutical sector.
