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Regulatory Affairs Specialist - FSP
Parexel International Corporation
China - Any Region - Home Based
Prepare and maintain regulatory dossiers for FP in dossier preparation, translation proof reading, binding and submission NDA. Support from RA perspective on the project during development and clinical trial.Qualifications1.Master, or bachelor in medicine related, and 1 year working experience, prefer from famous school, prefer global Pharma/CRO working experience.
2. English could be working language.
Job posted: 2021-09-25