IQVIA aims to realize a society where everyone can live healthier and more fulfilling lives by supporting those advancing healthcare with innovative solutions
Job Summary
IQVIA aims to realize a society where everyone can live healthier and more fulfilling lives by supporting those advancing healthcare with innovative solutions.
The FSP Medical Writing department handles various clinical development-related documents, offering extensive experience and a robust internal education system.
This position offers the opportunity to gain experience in document creation for a wide range of development items across pharmaceuticals, medical devices, and regenerative medicine.
Matching Summary
IQVIA aims to realize a society where everyone can live healthier and more fulfilling lives by supporting those advancing healthcare with innovative solutions.
Skills & Requirements
Must-have
Client SOP adherence
Clinical trial documentation
Japanese regulatory requirements
English reading and writing proficiency
Nice-to-have
Clinical pharmacology knowledge
PMDA interaction experience
Global environment collaboration
Key Requirements
4+ years of Medical Writing experience
Bachelor's or Master's degree in science
Pharmaceutical/medical basic knowledge
Understanding of drug development, GCP, ICH guidelines, and domestic drug regulations