17 set - Emilia-Romagna
IQVIA Italia
IQVIA Italia, on behalf of Chiesi Farmaceutici, seeks a Global Rare Disease Regulatory Affairs Specialist for EU and international submissions in a multinational context. The role focuses on preparing regulatory documents, coordinating regional filings, and ensuring quality submissions within timelines.
The ideal candidate has 2–3 years in EU/INT regulatory affairs, strong attention to detail, and fluent English, with the ability to work independently in a dynamic, international team based in
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