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 following client SOPs, 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 products, including pharmaceuticals, medical devices, and regenerative medicine, with advice available from internal medical and regulatory experts.
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
Clinical trial document creation
Post-marketing surveillance documents
English reading and writing proficiency
Japanese language fluency required
Nice-to-have
Clinical pharmacology knowledge
Experience with PMDA interactions
Global team collaboration
Key Requirements
4+ years of Medical Writing experience
Bachelor's or Master's degree in a science field
Understanding of drug development, GCP, ICH guidelines, and domestic drug regulations
Ability to proofread English documents and translate Japanese to English