Lead Regulatory Writer, Global Rare Diseases

07 set - Parma
Biopharma Careers

Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions.

Invii la sua candidatura dopo aver letto i requisiti di competenza e qualifica per questa posizione, riportati di seguito.

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. xbvzest
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Per questa posizione sono disponibili opzioni di lavoro a distanza/a casa.

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