Clinical Research Coordinator

About This Role

Coordinating and managing clinical research studies from participant recruitment to study closeout is the core of this role. The Clinical Research Coordinator ensures regulatory compliance, accurate data collection, and participant safety throughout the research process.

Responsibilities

• Recruit, screen, and enroll eligible study subjects
• Obtain informed consent under the guidance of the PI
• Coordinate and schedule participant visits, clinical procedures, and follow-up care from start-up to study closeout
• Collect, record, and manage accurate study data on source documents and electronic data capture (EDC) systems
• Resolve data queries in a timely manner
• Prepare and maintain regulatory binders, IRB submissions, and essential trial documentation
• Perform basic clinical measurements (vitals, ECGs)
• Process, store, or ship biological lab specimens according to protocol
• Monitor participant health and capture adverse events
• Facilitate sponsor monitoring visits and audits