Global Regulatory Writing Lead – Rare Diseases

31 ago - Parma
Chiesi

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.

Si candidi ora: legga i dettagli del lavoro scorrendo verso il basso. Verifichi di possedere le competenze necessarie prima di inviare la candidatura.

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

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