Clinical Research Coordinator

• Perform clinical and administrative coordination of sponsored clinical trials, research protocols/projects, and biospecimen collection studies
• Provide guidance to physicians, clinical staff, and research team members
• Coordinate study start-up, CTA/budget/CTMS review, IRB submissions, recruitment, screening, and enrollment
• Develop mechanisms to maximize subject adherence to research protocols
• Maintain source documentation and collect, complete, and submit case report forms through EDC
• Manage study drug/device accountability, monitor subjects, report AEs/SAEs, and support study closeout
• Facilitate quality assurance inspections and audits
• Act as liaison between sponsors and investigators and serve as primary protocol/project contact
• Develop and implement educational plans for research staff, investigators, and clinical staff
• Review protocol amendments, research-related orders, and study-specific workflows
• Ensure laboratory requirements are met for specimen procurement, collection, processing, and shipment
• Serve as Primary Research Coordinator across multiple sites and coordinate and track research activities
• Coach and mentor research team members and other personnel
• Assist with educational training plans and orientation
• Maintain competency in research computer applications
• Attend and participate in educational programs, meetings, and assigned committees
• Licensed nurses may use advanced assessment skills, provide professional nursing care to research patients, and support Research Coordinators with nursing activities as needed
• Provide coverage at multiple locations in Crystal Lake, Barrington, and Libertyville, Illinois

Clinical Research Coordinator jobs in United States

Research Coordinator – Oncology Clinical Trials