Crc Level 2

ICON plc

Ames, Iowa, USA
Onsite
Patient recruitment and enrollment
Study documentation and regulatory files
Data collection and entry
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.

Matching Summary

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

Skills & Requirements

Must-have

  • Patient recruitment and enrollment
  • Study documentation and regulatory files
  • Data collection and entry
  • Protocol compliance
  • Regulatory authorities and IRBs

Nice-to-have

  • Fostering an inclusive environment
  • Transforming clinical trial experience
  • Mentoring and staff development
  • Site level quality assurance
  • Well-being and work life balance

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter