Assoc Medical Writer (契約社員）

IQVIA

Science university degree preferred
Clinical trial document editing experience
Word document consistency checking skills
The role involves editing and performing quality control on documents created for clinical trials, PMS, and clinical research

Job Summary

  • The role involves editing and performing quality control on documents created for clinical trials, PMS, and clinical research.
  • Candidates will work within a comprehensive internal education system to handle various therapeutic areas and global studies.
  • The position offers a fully remote and flexible work environment with an initial one-year contract subject to renewal.

Matching Summary

The role involves editing and performing quality control on documents created for clinical trials, PMS, and clinical research.

Skills & Requirements

Must-have

  • Science university degree preferred
  • Clinical trial document editing experience
  • Word document consistency checking skills
  • Ability to work within strict timelines
  • Team collaboration for high-quality output

Nice-to-have

  • Experience with CSR and CTD QC
  • English document editing and QC background
  • Strong communication skills with mentors
  • Familiarity with PDF and Word handling

Key Requirements

  • University degree in science field
  • Basic knowledge of clinical trials
  • Proficiency in Word for document checks

Work Rights

Not specified

Tailored Resume

Cover Letter