Cta

ICON plc

Mexico City, Mexico
Clinical research experience
Clinical trial processes
Regulatory requirements
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.
  • 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 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 research experience
  • clinical trial processes
  • regulatory requirements
  • cross-functional teams
  • track and report metrics

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • work life balance opportunities
  • dedication to inclusion and belonging

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Prior experience or strong interest in clinical research
  • Knowledge of clinical trial regulations and guidelines
  • Excellent organizational and communication skills
  • Ability to work collaboratively in fast-paced environment
  • Willingness to travel approximately 10%

Work Rights

Not specified

Tailored Resume

Cover Letter