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 pharmacy degree required
Knowledge of gcp and ich guidelines
The role involves creating clinical trial documents such as protocols, summary reports, and technical documents for various therapeutic areas

Job Summary

  • The role involves creating clinical trial documents such as protocols, summary reports, and technical documents for various therapeutic areas.
  • Candidates will work in a flexible remote environment with access to comprehensive internal training systems and expert advice from doctors and regulatory specialists.
  • The position offers opportunities to contribute to the development of innovative medicines and medical devices while supporting patient outcomes globally.

Matching Summary

The role involves creating clinical trial documents such as protocols, summary reports, and technical documents for various therapeutic areas.

Salary

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

Skills & Requirements

Must-have

  • Medical Writing practical experience
  • Science or Pharmacy degree required
  • Knowledge of GCP and ICH guidelines
  • Understanding of Japanese drug regulations
  • English reading and writing proficiency

Nice-to-have

  • Clinical pharmacology knowledge
  • Experience with global medical writing
  • Collaboration with internal medical experts

Key Requirements

  • Bachelor's or Master's degree in Science/Pharmacy
  • Minimum practical experience in Medical Writing
  • Fluency in Japanese and English
  • Understanding of GPSP and domestic regulations

Work Rights

Not specified

Tailored Resume

Cover Letter