Clinical Affairs Specialist

AbbVie

Tokyo, Japan
Clinical trial management system
Gcp compliance
Study document management
This role is responsible for managing study documentation and operational progress using Clinical Trial Management System

Job Summary

  • This role is responsible for managing study documentation and operational progress using Clinical Trial Management System.
  • The position oversees documentation and study management support across clinical studies, ensuring compliance with regulations and SOPs.
  • We seek individuals who can maintain the highest level of quality in clinical studies while proactively addressing new challenges.

Matching Summary

This role is responsible for managing study documentation and operational progress using Clinical Trial Management System.

Skills & Requirements

Must-have

  • Clinical Trial Management System
  • GCP compliance
  • Study document management

Nice-to-have

  • Team collaboration skills
  • Process improvement mindset
  • Medical terminology knowledge

Key Requirements

  • Bachelor’s degree in science/health-related field
  • >2 Years of experience in Field Clinical Research Associate
  • Fluent in English and Japanese

Work Rights

Not specified

Tailored Resume

Cover Letter