メディカルライター（fso Medical Writer/ Iqvia Services）

IQVIA

Japan
Not specified; salary determined by compyny st + a...
Medical writing practical experience
Science or medicine degree required
Pharmaceutical development knowledge
The role involves creating clinical trial documents, regulatory submission materials, and scientific reports for pharmaceutical clients

Job Summary

  • The role involves creating clinical trial documents, regulatory submission materials, and scientific reports for pharmaceutical clients.
  • Candidates must possess a science or medical degree along with practical Medical Writing experience beyond translation.
  • The position offers a fully remote work arrangement with flexible hours and access to a comprehensive benefits package.

Matching Summary

The role involves creating clinical trial documents, regulatory submission materials, and scientific reports for pharmaceutical clients.

Salary

Not specified; Salary determined by company standards; Bonus and overtime pay available

Skills & Requirements

Must-have

  • Medical Writing practical experience
  • Science or Medicine degree required
  • Pharmaceutical development knowledge
  • GCP and ICH guideline understanding
  • Japanese domestic regulatory knowledge
  • English reading and writing proficiency

Nice-to-have

  • Clinical pharmacology knowledge
  • Experience with medical devices
  • Regenerative medicine background
  • Global medical writing environment
  • Access to internal expert advice

Key Requirements

  • Medical Writing practical experience (translation only excluded)
  • Bachelor's or Master's degree in Science/Medicine
  • Fluency in Japanese and English
  • Understanding of GPSP and domestic drug regulations

Work Rights

Not specified

Tailored Resume

Cover Letter