Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions.
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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. xkiyazw
Per questa posizione sono disponibili opzioni di lavoro a distanza/a casa.
📌 Lead Regulatory Writer, Global Rare Diseases (Remote) (Parma)
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📍 Parma