Remote Regulatory Affairs Consultant – CMC & Post-Approval

Parexel is looking for an experienced Regulatory Affairs Consultant to join our team on a client dedicated project. The role can be office or home based in various European locations, with a focus on post-approval CMC activities for biological and plasma products.

You will develop submission strategies, assess change controls, coordinate submissions, and manage regulatory information systems to ensure timely global submissions and regulatory compliance.

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