Senior Medical Writer

ICON

Tokyo, Japan
Hybrid
Medical writing for clinical research
Regulatory document preparation
Clinical trial data interpretation
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence in clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence in clinical development.
  • The Senior Medical Writer will lead the preparation and review of clinical study documents, collaborate with multiple departments, and mentor junior staff to ensure high-quality scientific communication.
  • ICON offers competitive salary and benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence in clinical development.

Skills & Requirements

Must-have

  • Medical writing for clinical research
  • Regulatory document preparation
  • Clinical trial data interpretation
  • Collaboration with cross-functional teams
  • Compliance with regulatory guidelines
  • Mentoring junior medical writers

Nice-to-have

  • Strong interpersonal and communication skills
  • Ability to work in fast-paced environment
  • Fostering culture of excellence and learning
  • Experience with publication planning
  • Multilingual document creation and review

Key Requirements

  • Advanced degree in Life Sciences or related field
  • 3-5 years medical writing experience in pharma or CRO
  • Proficiency in clinical trial data analysis
  • Knowledge of ICH-GCP, FDA, EMA regulations
  • Experience interacting with regulatory agencies
  • University graduate in medical or life sciences
  • Minimum 3 years medical writing in pharma or CRO

Work Rights

Not specified

Tailored Resume

Cover Letter