Bp-clinical Trial Associate (cta)

ICON Clinical Research, LP

Taipei, Taiwan
On-site
Clinical trial administration
Regulatory requirements
Study documentation
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
  • Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
  • In addition to your competitive salary, ICON offers a range of additional benefits.

Matching Summary

As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical trial administration
  • regulatory requirements
  • study documentation
  • cross-functional teams
  • clinical trial metrics

Nice-to-have

  • fast-paced environment
  • attention to detail
  • inclusive environment
  • innovative treatments

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Prior experience or strong interest in clinical research
  • Knowledge of clinical trial processes, regulations, and guidelines
  • Willingness to travel as required (approximately 10%)

Work Rights

Not specified

Tailored Resume

Cover Letter