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

IQVIA

Japan
Not specified; salary determined by compyny regula...
5+ years medical writing experience
Clinical trial document creation
Gcp and ich guideline knowledge
The role involves leading the creation and review of clinical trial documents such as protocols, summary reports, and common technical documents

Job Summary

  • The role involves leading the creation and review of clinical trial documents such as protocols, summary reports, and common technical documents.
  • Candidates will work in a global environment with access to internal advice from doctors and regulatory experts.
  • The position offers flexible working hours and full remote work options across Japan.

Matching Summary

The role involves leading the creation and review of clinical trial documents such as protocols, summary reports, and common technical documents.

Salary

Not specified; Salary determined by company regulations; Bonus available

Skills & Requirements

Must-have

  • 5+ years Medical Writing experience
  • Clinical trial document creation
  • GCP and ICH guideline knowledge
  • Japanese domestic regulatory knowledge
  • English reading and writing skills

Nice-to-have

  • Clinical pharmacology business experience
  • Global medical writing environment
  • Mentoring junior staff capabilities

Key Requirements

  • Bachelor's or Master's degree in Science
  • Pharmacy, Medicine, or Statistics background
  • TOEIC score of 730 or higher
  • Fluency in Japanese required

Work Rights

Not specified

Tailored Resume

Cover Letter