Global Rare Disease Regulatory Affairs Specialist EU

6 giorni fa

Rome, Lazio, Italia Altro Tempo pieno

IQVIA, on behalf of Chiesi Farmaceutici, is seeking a Global Rare Disease Regulatory Affairs Specialist EU&INT to join our international team in Rome, Italy.
The role involves preparing regulatory documents for submissions, coordinating with consultants and affiliates, reviewing submission documents, and guiding colleagues. 2-3 years in EU/INT regulatory affairs, lifecycle management experience, and fluent English are required.