15 set - Parma
IQVIA Italia
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Global Rare Disease Regulatory Affairs Specialist EU∫ to join an exciting working environment in a dynamic and international atmosphere. Main regulatory responsibilities : Under guidance of the manager, prepares, compiles, and maintains regulatory documents to support a broad range
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