Cta - Sponsor Dedicated

ICON Clinical Research, LP

Fully remote
Assist in trial coordination and administration
Maintain clinical trial documentation
Support study-related material preparation
As a Clinical Trial Associate 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 Associate 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.
  • Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
  • Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Matching Summary

As a Clinical Trial Associate 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

  • Assist in trial coordination and administration
  • Maintain clinical trial documentation
  • Support study-related material preparation
  • Facilitate cross-functional team communication
  • Track and report clinical trial metrics

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Contribute to advancing treatments

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • 1 year or less clinical research experience
  • Knowledge of clinical trial processes
  • Excellent organizational and communication skills
  • Ability to work collaboratively in fast-paced environment

Work Rights

Not specified

Tailored Resume

Cover Letter