Clinical Research Coordinator

The Clinical Research Coordinator will coordinate clinical research and quality improvement efforts within the Division of Pain Medicine under the Principal Investigator and/or designee’s guidance.

Requirements

• Coordinates study operations, implementing processes and procedures to meet protocol requirements and study goals.
• Recruit, consent, and enroll participants; evaluate eligibility and respond to study-related inquiries.
• Ensure regulatory compliance, including IRB submissions, maintaining regulatory binders, monitoring adverse events, and managing protocol amendments.
• Coordinate multi-center and site activities, serve as liaison with stakeholders, and ensure accurate data collection, database maintenance, and timely reporting.
• Manage study finances, including budgeting, expense monitoring, financial reporting, and subrecipient oversight.
• Support research dissemination and development by preparing reports, abstracts, manuscripts, presentations, training materials, and grant applications.