Cta

ICON Clinical Research, LP

Mexico City, Mexico
Clinical trial administration
Regulatory compliance
Documentation management
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.
  • Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

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 compliance
  • documentation management
  • cross-functional team collaboration
  • clinical trial metrics tracking

Nice-to-have

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

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
  • Ability to work collaboratively in a fast-paced environment
  • Willingness to travel approximately 10%

Work Rights

Not specified

Tailored Resume

Cover Letter