Clinical Research Coordinator I/II/III

About the role

The University of Arkansas for Medical Sciences is seeking Clinical Research Coordinators (I, II, and III) to support a variety of clinical studies. The role involves managing day‑to‑day study operations, ensuring regulatory compliance, and facilitating communication between investigators, participants, and study sponsors.

Key responsibilities

• Coordinate all aspects of clinical trial activities, including participant recruitment, scheduling, and follow‑up.
• Maintain accurate study documentation and source records in accordance with Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements.
• Prepare and submit regulatory documents, consent forms, and study reports.
• Monitor study progress, track data collection, and ensure timely entry into clinical trial management systems.
• Collaborate with investigators, sponsors, and cross‑functional teams to resolve study issues.

Required profile

• Bachelor’s degree in a health‑related field or equivalent experience.
• Relevant experience in clinical research, with level‑specific expectations for I, II, or III positions.
• Understanding of GCP, IRB processes, and federal regulations governing human subjects research.
• Strong organizational abilities and attention to detail.

Required skills

• Proficiency with clinical trial management software.
• Knowledge of Good Clinical Practice (GCP) guidelines.
• Experience preparing IRB submissions and regulatory documentation.

What we offer

• Comprehensive medical, dental, and vision insurance for eligible staff and families.
• Retirement plan with up to 10% employer match.
• Basic life insurance coverage up to $50,000.
• Paid holiday, vacation, and sick leave.
• Education discounts for staff and dependents.
• Merchant discounts, concierge prescription delivery, and career training opportunities.