Clinical Trials Assistant (cta)

IQVIA

Taipei, Taiwan
Trial master file delivery
Clinical documents and systems
Clinical documentation and reports
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.
  • Act as a central contact for the clinical team for designated project communications and documentation.

Matching Summary

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

Skills & Requirements

Must-have

  • Trial Master File delivery
  • clinical documents and systems
  • clinical documentation and reports
  • tracking and management of CRFs
  • project communications correspondence

Nice-to-have

  • effective time management
  • establish and maintain relationships
  • awareness of regulatory requirements

Key Requirements

  • High School Diploma or equivalent
  • 3 years administrative support experience
  • Computer skills Microsoft Word, Excel, PowerPoint
  • Written and verbal communication skills English
  • Awareness of GCP and ICH guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter