Global Regulatory Writing Lead – Rare Diseases

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7kinfp

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.
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The role combines writing mastery with cross-functional leadership and regulatory strategy expertise.
The role can be based at the Parma HQ xysqume or one of Chiesi's European affiliates, with flexible working arrangements and a comprehensive compensation
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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7kinfp