Crc Level 2

ICON plc

Ames, Iowa, USA
Onsite
Protocol compliance
Regulatory standards
Study documentation maintenance
The CRC 2 will actively recruit and promote our service to suitable participants and sponsor representatives

Job Summary

  • The CRC 2 will actively recruit and promote our service to suitable participants and sponsor representatives.
  • Leading the coordination and implementation of clinical trial activities, including patient recruitment, screening, enrollment, and follow-up, ensuring compliance with protocol requirements and regulatory standards.
  • 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

The CRC 2 will actively recruit and promote our service to suitable participants and sponsor representatives.

Skills & Requirements

Must-have

  • Protocol compliance
  • Regulatory standards
  • Study documentation maintenance
  • Data accuracy and completeness
  • Electronic Data Capture (EDC) systems

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Transforming clinical trial experience
  • Work-life balance opportunities
  • Global Employee Assistance Programme

Key Requirements

  • Minimum 2 years experience
  • Bachelor's degree or relevant experience
  • Proficiency in Microsoft Office suite
  • Experience with EDC and CTMS systems preferred

Work Rights

Not specified

Tailored Resume

Cover Letter