Experteer Italy seeks a candidate to author and manage regulatory documents that translate data into compliant submissions. This role involves overseeing document development for marketing applications and guiding both external writers and internal experts.
The ideal candidate will have a life science degree (PhD or PharmD preferred), relevant regulatory writing experience, and the ability to lead cross-functional teams effectively, contributing to the regulatory strategy in a mission-driven environment.
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📌 Principal Regulatory Writer, Rare Diseases — Lead (Parma)
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📍 Parma
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