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.
As a Medical Writer, you will be responsible for creating various clinical development-related documents, including protocols, CSRs, and CTDs, following client SOPs.
This position offers the opportunity to gain extensive experience across a wide range of development products in 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
Clinical trial documentation creation
Post-marketing surveillance documents
Regulatory guideline comprehension
English reading and writing proficiency
Nice-to-have
Clinical pharmacology knowledge
PMDA interaction experience
Global team collaboration
Key Requirements
4+ years of Medical Writing experience
Bachelor's or Master's degree in science
Pharmaceutical and medical basic knowledge
Understanding of GCP, ICH guidelines, and domestic drug regulations