Crc Level 2

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Ames, Iowa, USA
Onsite
Clinical trial coordination
Patient recruitment and enrollment
Regulatory compliance management
The CRC 2 ensures the safety of participants and coordinates multiple clinical studies autonomously according to protocol

Job Summary

  • The CRC 2 ensures the safety of participants and coordinates multiple clinical studies autonomously according to protocol.
  • ICON offers competitive salary and a range of benefits focused on well-being and work life balance for employees and their families.
  • ICON is dedicated to providing an inclusive and accessible environment and is committed to equal employment opportunity without discrimination.

Matching Summary

The CRC 2 ensures the safety of participants and coordinates multiple clinical studies autonomously according to protocol.

Skills & Requirements

Must-have

  • clinical trial coordination
  • patient recruitment and enrollment
  • regulatory compliance management
  • data entry and query resolution
  • study documentation maintenance
  • electronic data capture systems

Nice-to-have

  • mentoring junior staff
  • clinical trial management systems experience
  • strong organizational skills
  • excellent communication skills
  • inclusive work environment
  • work life balance focus

Key Requirements

  • Bachelor's degree or relevant experience
  • Minimum 2 years clinical research experience
  • Proficiency in study coordination and data management

Work Rights

Not specified

Tailored Resume

Cover Letter