09 set - Campo di Ne
Parexel International
Parexel International is seeking a Senior Regulatory Affairs Associate to join our team on a client-dedicated project. This role focuses on post-approval CMC regulatory activities for biological and vaccines products, with options for office or home-based work across Europe.
You will develop submission strategies, assess change controls, and coordinate cross-department submissions while ensuring global regulatory compliance. Fluent English is required.
J-18808-Ljbffr
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