Senior CMC Regulatory Affairs Consultant (Biologics)

Parexel is seeking an experienced Regulatory Affairs Consultant CMC Author to support our client. The role focuses on CMC authoring for initial submissions and lifecycle management, with emphasis on biologics.

The position can be home or office based across European locations, offering flexibility for experienced professionals. Qualified candidates have 10+ years in CMC and regulatory affairs, strong regulatory knowledge (ICH, EU/US), and experience with document management systems.

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