Principal Regulatory Writer, Rare Diseases — Lead

31 lug - Parma
Experteer Italy

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.
#J-*****-Ljbffr

Clinical Trials Operations Specialist — Study Lead Support

20 ago - Bologna
Alfasigma

Responsabile magazzino pharma

20 ago - Salerno
Adecco

Ricevi nuove offerte di lavoro

Crea una Job Alert gratuita per principal regulatory writer, rare diseases — lead / parma

Addetto/a montaggio meccanico...

20 ago - Buia
Adecco

Senior Lean and Continuous Improvement Engineer (m/f/d)

20 ago - Milano
Fiamm Energy Technology