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

IQVIA Inc

Japan
Not specified; salary determined by compyny st + a...
5+ years medical writing experience
Science degree required
Gcp and ich guidelines knowledge
The role involves creating and reviewing clinical trial documents such as protocols and global study reports for pharmaceutical clients

Job Summary

  • The role involves creating and reviewing clinical trial documents such as protocols and global study reports for pharmaceutical clients.
  • Candidates will manage project timelines, personnel, and budgets while providing guidance to junior team members.
  • The position offers a fully remote work arrangement with access to internal experts including doctors and regulatory specialists.

Matching Summary

The role involves creating and reviewing clinical trial documents such as protocols and global study reports for pharmaceutical clients.

Salary

Not specified; Salary determined by company standards; Bonus available

Skills & Requirements

Must-have

  • 5+ years Medical Writing experience
  • Science degree required
  • GCP and ICH guidelines knowledge
  • Japanese domestic drug regulations
  • English reading and writing skills

Nice-to-have

  • Clinical pharmacology background
  • Global medical writing environment
  • Mentoring junior staff
  • Project progress management
  • Patient-centric mission focus

Key Requirements

  • Bachelor's or Master's degree in Science
  • Minimum 5 years of Medical Writing experience
  • TOEIC score of 730 or higher
  • Fluency in Japanese language
  • Knowledge of GCP and ICH guidelines

Work Rights

Not specified

Tailored Resume

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