Lead Regulatory Writer, Global Rare Diseases

2 ore fa

ravenna, emilia romagna, Italia Biopharma Careers Tempo pieno

Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.

The role requires a life science degree, fluency in English, and strong experience in regulatory writing across development stages. Location can be Parma HQ or Europe affiliates, with competitive compensation and benefits.