Kansas Licensed Clinical Research Coordinator

Job Summary

A company is looking for a Clinical Research Coordinator II.

Key Responsibilities

• Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines
• Schedules subject visits and performs all defined study activities, ensuring patient safety and compliance
• Maintains accurate patient records and source documents, ensuring all information is up to date

Required Qualifications

• Bachelor's degree or equivalent in the clinical/medical field
• Valid nursing license (RN, LVN, LPN) registered with local health care authority
• Minimum of 2 years of relevant clinical research experience
• Solid understanding of clinical research processes including GCP and informed consent
• Proficiency in basic computer applications