Assoc Medical Writer (契約社員）

IQVIA Inc

Japan
Science degree required
Clinical trial document qc experience
Japanese document editing skills
The role involves editing and quality controlling documents created for clinical trials, PMS, and clinical research

Job Summary

  • The role involves editing and quality controlling documents created for clinical trials, PMS, and clinical research.
  • Candidates must adhere to internal SOPs or client-specific SOPs while delivering high-quality work within set deadlines.
  • The position offers a fully remote work environment with flexible hours under a renewable one-year contract.

Matching Summary

The role involves editing and quality controlling documents created for clinical trials, PMS, and clinical research.

Skills & Requirements

Must-have

  • Science degree required
  • Clinical trial document QC experience
  • Japanese document editing skills
  • Word proficiency for consistency checks
  • Ability to meet strict timelines

Nice-to-have

  • CTD or CSR QC experience
  • English document editing experience
  • Team collaboration skills
  • Experience with global studies
  • Knowledge of medical terminology

Key Requirements

  • University degree in science field
  • Experience with clinical trial documents
  • Proficiency in Japanese and English editing
  • Strong attention to detail for data consistency

Work Rights

Not specified

Tailored Resume

Cover Letter