Clinical Research Coordinator

ICON

Wilmington, NC, United States
Onsite
Clinical trial management system skills
Participant recruitment and screening
Data entry in electronic data capture
The Clinical Research Coordinator plays a key role in transforming the clinical trial experience for patients and sponsors by ensuring safety and meeting study priorities

Job Summary

  • The Clinical Research Coordinator plays a key role in transforming the clinical trial experience for patients and sponsors by ensuring safety and meeting study priorities.
  • ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.
  • ICON is committed to fostering an inclusive and accessible environment and provides equal employment opportunities without discrimination.

Matching Summary

The Clinical Research Coordinator plays a key role in transforming the clinical trial experience for patients and sponsors by ensuring safety and meeting study priorities.

Skills & Requirements

Must-have

  • Clinical Trial Management System skills
  • Participant recruitment and screening
  • Data entry in Electronic Data Capture
  • Perform clinical protocol technical procedures
  • Study start-up and documentation
  • Communication with investigators and sponsors

Nice-to-have

  • Mentoring and staff development
  • Strong attention to detail
  • Building relationships with clinical teams
  • Interest in clinical research career
  • Inclusive and diverse workplace culture

Key Requirements

  • Bachelor's Degree
  • 1+ years clinical research coordinator experience
  • Work authorization in the United States

Work Rights

Not specified

Tailored Resume

Cover Letter