Clinical Trial Assistance (ssu)

ICON

Taipei, Taiwan
Regulatory document management
Submission dossier preparation
Study start-up coordination
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 innovative 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 innovative treatments and therapies.
  • ICON offers a diverse and inclusive culture that rewards high performance and nurtures talent, providing competitive salary and a range of benefits focused on well-being and work-life balance.
  • The role involves supporting regulatory submissions to Ethics Committees and Health Authorities, maintaining Trial Master File readiness, and ensuring compliance with ICH-GCP and local regulations.

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 innovative treatments and therapies.

Skills & Requirements

Must-have

  • regulatory document management
  • submission dossier preparation
  • study start-up coordination
  • ICH-GCP compliance
  • clinical trial administration
  • document version control

Nice-to-have

  • collaborative work environment
  • attention to detail
  • continuous improvement culture
  • support meeting logistics
  • translation coordination
  • fast-paced environment

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Prior experience in IRB initial submission
  • Knowledge of ICH-GCP and regulatory requirements
  • Ability to work collaboratively in fast-paced environment

Work Rights

Not specified

Tailored Resume

Cover Letter