Clinical Research Coordinator III

Clinical Research Coordinator III

Prepares grant applications, manuscripts, Institutional Review Board (IRB) applications, research papers, and assists with complex research papers. Audits research studies, monitors study budgets, resolves complex data collection issues, and implements protocol-specific study recruitment plans. Trains staff and oversees student workers; leads team meetings. Monitors study budgets and orders supplies.

• Interfaces with clinical staff to identify patients eligible for clinical trials
• Collects, maintains, and stores all relevant clinical data, case report forms, and regulatory binders in accordance with the study sponsor and all regulatory bodies.
• Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules
• Conducting study visits, including vital signs, blood draw and processing. Includes the collection, labeling, storage and transport of all specimens
• Conducting monitor visits and resolution of data queries in a timely manner

Must be able to sit or stand for prolonged periods of time.