Clinical Trials Assistant, Sponsor Dedicated

IQVIA UK

Seoul, South Korea
Trial master file management
Clinical document maintenance
Effective communication skills
The role involves assisting Clinical Research Associates and Regulatory teams with clinical documentation

Job Summary

  • The role involves assisting Clinical Research Associates and Regulatory teams with clinical documentation.
  • You will coordinate the tracking and management of Case Report Forms and clinical data flow.
  • IQVIA is committed to integrity in the hiring process and values professionalism.

Matching Summary

The role involves assisting Clinical Research Associates and Regulatory teams with clinical documentation.

Skills & Requirements

Must-have

  • Trial Master File management
  • Clinical document maintenance
  • Effective communication skills

Nice-to-have

  • Team collaboration
  • Time management skills
  • Basic regulatory knowledge

Key Requirements

  • BA/BS in Life Sciences
  • At least 1 year of clinical research experience
  • Knowledge of Good Clinical Practice

Work Rights

Not specified

Tailored Resume

Cover Letter