Principal Regulatory Writer, Rare Diseases — Lead

31 lug - Parma
Experteer Italy

pExperteer 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. /ppThe 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. /p #J-18808-Ljbffr

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