Clinical Research Coordinator

ICON Broadbean

Wilmington, North Carolina, United States
Onsite
Clinical trial management system
Participant recruitment
Data collection and documentation
The CRC ensures the safety of participants and promotes the mission of Accellacare

Job Summary

  • The CRC ensures the safety of participants and promotes the mission of Accellacare.
  • This role involves recruiting suitable participants and coordinating multiple studies.
  • ICON offers a diverse culture that rewards high performance and nurtures talent.

Matching Summary

The CRC ensures the safety of participants and promotes the mission of Accellacare.

Skills & Requirements

Must-have

  • Clinical Trial Management System
  • Participant recruitment
  • Data collection and documentation

Nice-to-have

  • Attention to detail
  • Mentoring skills
  • Strong communication skills

Key Requirements

  • Bachelor's Degree
  • 1+ years of experience as a clinical research coordinator

Work Rights

Not specified

Tailored Resume

Cover Letter