Principal Regulatory Writer, Rare Diseases — Lead

03 ago - Parma
Experteer Italy

Experteer Italy seeks a candidate to author and manage regulatory documents that translate data into compliant submissions.
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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 xysqume lead cross-functional teams effectively, contributing to the regulatory strategy in a mission-driven environment.

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