Clinical Research Coordinator – Onsite in Okinawa, Japan

About the role

Arcetyp LLC is seeking a qualified Clinical Research Coordinator to work onsite in Okinawa, Japan. The role supports federal and military research contracts by managing data collection and ensuring compliance with study protocols.

Key responsibilities

• Coordinate and participate in clinical research studies, handling complex data collection, compilation, documentation, and analysis.
• Implement procedures for gathering data from patient charts, medical records, interviews, questionnaires, diagnostic tests, and other sources.
• Assist in establishing guidelines for clinical data collection and study administration.

Required profile

• Bachelor’s degree from an accredited institution and at least 2 years recent experience as a Clinical Research Coordinator, or current certification (CCTI, CCRC, or CCRP).
• 2‑4 years of monitoring experience in a clinical research environment and experience with Institutional Review Board (IRB) processes.
• Active U.S. secret security clearance and U.S. citizenship.
• Ability to complete CITTI research subject protection training within one month of start date.

Required skills

• Proficiency with Windows operating systems.
• Strong command of Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).

What we offer

• Full‑time salaried position with a competitive compensation and benefits package.
• Opportunity to work on government‑contracted clinical research projects in an international setting.