Clinical Research Coordinator, Sponsor Dedicated

ICON Broadbean

Fort Worth, TX, United States
Clinical coordination work
Participant recruitment and enrollment
Collecting and maintaining clinical trial data
As a Clinical Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
  • Your role will involve delivering clinical coordination 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 Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical coordination work
  • participant recruitment and enrollment
  • collecting and maintaining clinical trial data
  • managing study-related documentation
  • support and guidance to study participants

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • work life balance opportunities

Key Requirements

  • Bachelor's degree in relevant field
  • Previous clinical research experience preferred
  • Knowledge of clinical research regulations
  • Strong organizational, communication, interpersonal skills
  • Detail-oriented with multitasking ability
  • Ophthalmology experience preferred
  • COA certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter