Clinical Trials Assistant, Sponsor Dedicated

IQVIA

Seoul, South Korea
Trial master file management
Clinical documentation handling
Tracking clinical data flow
Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery

Job Summary

  • Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.
  • Assist Clinical Research Associates and Regulatory and Start-Up teams with maintaining clinical documents and systems.
  • Coordinate the tracking and management of Case Report Forms, queries, and clinical data flow.

Matching Summary

Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.

Skills & Requirements

Must-have

  • Trial Master File management
  • clinical documentation handling
  • tracking clinical data flow
  • project timeline adherence
  • site compliance tracking

Nice-to-have

  • effective client relationships
  • strong organizational skills
  • team collaboration

Key Requirements

  • BA/BS degree or equivalent experience
  • 1 year CTA-related experience
  • Minimum 1 year clinical research experience
  • Proficiency in Microsoft Word, Excel, PowerPoint
  • Good command of English language
  • Basic knowledge of GCP and ICH guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter