IQVIA, on behalf of Chiesi Farmaceutici, is seeking a Global Rare Disease Regulatory Affairs Specialist for EU and INT in Rome, Italy. The role supports submissions to regulatory authorities and lifecycle management for global rare disease products, collaborating with consultants, partners, and affiliates.
Requirements include 2–3 years in regulatory affairs at a multinational company, strong attention to detail, and advanced English.
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📌 Global Rare Disease Regulatory Specialist EU&INT (Roma)
🏢 Altro
📍 Roma