Clinical Research Coordinator

ICON plc

Wilmington, North Carolina, United States
Onsite
Clinical trial management system
Recruitment planning
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.
  • You will actively recruit suitable participants and perform tasks to coordinate multiple studies.
  • ICON fosters an inclusive environment and offers a range of benefits focused on well-being.

Matching Summary

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

Skills & Requirements

Must-have

  • Clinical Trial Management System
  • Recruitment planning
  • Data collection and documentation

Nice-to-have

  • Mentoring and staff development
  • Strong communication skills
  • Attention to detail

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter