IQVIA, on behalf of Chiesi Farmaceutici, is seeking a Global Rare Disease Regulatory Affairs Specialist EU∫ 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.
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📌 Global Rare Disease Regulatory Affairs Specialist EU & Intl (Roma)
🏢 Altro
📍 Roma