Clinical Research Coordinator 2

ICON plc

Ames, Iowa, USA
Onsite
Clinical trial activities coordination
Data management proficiency
Regulatory compliance knowledge
The CRC 2 ensures the safety of our participants and promotes the mission of Accellacare

Job Summary

  • The CRC 2 ensures the safety of our participants and promotes the mission of Accellacare.
  • You will actively recruit and promote our service to suitable participants and sponsor representatives.
  • ICON offers a range of additional benefits designed to support well-being and work-life balance.

Matching Summary

The CRC 2 ensures the safety of our participants and promotes the mission of Accellacare.

Skills & Requirements

Must-have

  • Clinical trial activities coordination
  • Data management proficiency
  • Regulatory compliance knowledge

Nice-to-have

  • Strong organizational skills
  • Excellent communication abilities
  • Mentoring junior staff

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum of 2 years experience in clinical research
  • Proficiency in Microsoft Office suite

Work Rights

Not specified

Tailored Resume

Cover Letter