Clinical Trial Associate

ICON Clinical Research, LP

Beijing, China
Clinical trial administration
Study file maintenance
Regulatory 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.
  • Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
  • 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

  • clinical trial administration
  • study file maintenance
  • regulatory compliance
  • cross-functional team collaboration
  • tracking and reporting metrics

Nice-to-have

  • fostering inclusive environment
  • driving innovation and excellence
  • advancement of treatments and therapies
  • well-being and work life balance

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Prior experience in clinical research
  • Knowledge of clinical trial processes
  • Excellent organizational skills
  • Ability to work collaboratively

Work Rights

Not specified

Tailored Resume

Cover Letter