Clinical Study Coordinator

ICON Clinical Research, LP

San Antonio, TX, United States
Participant recruitment and enrollment
Data collection and maintenance
Study-related documentation management
As a Clinical Research Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Research Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
  • 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 play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • Participant recruitment and enrollment
  • Data collection and maintenance
  • Study-related documentation management
  • Compliance with study protocols
  • Support study participants

Nice-to-have

  • Inclusive and diverse team environment
  • Advancement of innovative treatments
  • Focus on well-being and work-life balance

Key Requirements

  • Bachelor's degree in relevant discipline
  • Previous clinical research experience preferred
  • Knowledge of clinical research regulations
  • Strong organizational skills
  • Ability to manage multiple tasks

Work Rights

Not specified

Tailored Resume

Cover Letter