Clinical Trial Assistance (ssu)

ICON plc

Taipei, Taiwan
Regulatory document management
Submission dossier preparation
Ich-gcp compliance
As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies

Job Summary

  • As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.
  • Provide administrative and operational support to the Study Start-Up team, with a primary focus on regulatory document management and submission dossier preparation.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.

Skills & Requirements

Must-have

  • regulatory document management
  • submission dossier preparation
  • ICH-GCP compliance
  • essential document verification
  • CTMS record maintenance
  • Trial Master File readiness

Nice-to-have

  • continuous improvement culture
  • collaborative work environment
  • advancement of innovative treatments

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Prior experience in IRB initial submission
  • Excellent organizational and communication skills
  • Ability to work in a fast-paced environment
  • Attention to detail

Work Rights

Not specified

Tailored Resume

Cover Letter