Clinical Research Coordinator I/II/III

About the role

The Clinical Research Coordinator supports investigators in the planning, execution, and reporting of clinical studies at the University of Arkansas for Medical Sciences. This position ensures compliance with regulatory requirements and facilitates high‑quality data collection.

Key responsibilities

• Assist principal investigators with study start‑up activities, including protocol review and IRB submissions.
• Maintain study documentation, regulatory binders, and electronic records in accordance with GCP and institutional policies.
• Coordinate participant recruitment, scheduling, and follow‑up visits.
• Collect, enter, and verify study data, ensuring accuracy and completeness.
• Monitor study progress, track milestones, and report status to the research team.
• Facilitate communication between study sites, sponsors, and internal departments.

Required profile

• Bachelor’s degree in a health‑related field or equivalent experience.
• Experience in clinical research coordination, preferably in a university or hospital setting.
• Knowledge of Good Clinical Practice (GCP), IRB processes, and federal regulations.
• Strong organizational and communication skills.

Required skills

What we offer

• Comprehensive medical, dental, and vision insurance.
• Retirement plan with up to 10% employer match.
• Paid holiday, vacation, and sick leave.
• Education discounts for staff and dependents.
• Career training, educational opportunities, and merchant discounts.