シニアメディカルライター(sr. Medical Writer/ Iqvia Services)

IQVIA UK

Multiple Locations, Japan
Medical writing experience 5+ years
Clinical trial documentation
Global trial protocol amendments
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 Medical Writing department offers diverse documentation experience across various therapeutic areas and provides a robust internal education system.
  • This position offers the opportunity to experience document creation for a wide range of development items in pharmaceuticals, medical devices, and regenerative medicine, and to work in a global environment.

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

  • Medical Writing experience 5+ years
  • Clinical trial documentation
  • Global trial protocol amendments
  • Regulatory compliance
  • English reading and writing proficiency

Nice-to-have

  • Experience in clinical pharmacology
  • Mentoring junior staff
  • Cross-functional collaboration

Key Requirements

  • Medical Writing experience 5+ years
  • Bachelor's or Master's degree in science
  • Understanding of drug development, GCP, ICH guidelines
  • Knowledge of domestic pharmaceutical regulations
  • Basic knowledge of pharmacology, medicine, statistics
  • English proficiency (TOEIC 730+)
  • Fluency in Japanese

Work Rights

Not specified

Tailored Resume

Cover Letter