Global Regulatory Writing Lead – Rare Diseases

Chiesi Global Rare Diseases in Parma is seeking a Principal Regulatory Writer to lead the development of regulatory documents across the drug development lifecycle, translating data into compliant submissions for FDA, EMA, and other authorities.

The role combines writing mastery with cross-functional leadership and regulatory strategy expertise. The role can be based at the Parma HQ or one of Chiesi's European affiliates, with flexible working arrangements and a comprehensive compensation

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