Clinical Trials Assistant (cta)

IQVIA UK

Taipei, Taiwan
Trial master file (tmf) maintenance
Clinical document management
Regulatory and start-up support
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 updating and maintaining clinical documents and systems.
  • Act as a central contact for the clinical team for designated project communications and correspondence.

Matching Summary

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

Skills & Requirements

Must-have

  • Trial Master File (TMF) maintenance
  • Clinical document management
  • Regulatory and Start-Up support
  • Clinical Trial Supplies tracking
  • Case Report Forms (CRFs) tracking

Nice-to-have

  • Effective time management
  • Organizational skills
  • Maintain effective working relationships
  • Awareness of GCP and ICH guidelines

Key Requirements

  • High School Diploma or equivalent
  • 3 years administrative support experience
  • Computer skills (Word, Excel, PowerPoint)
  • Written and verbal communication skills
  • Good command of English language
  • Awareness of applicable regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter