Clinical Research Coordinator - Spartanburg, SC

Clinical Research Coordinator coordinates with the Principal Investigator, department, and administration to ensure trial activities comply with Federal Regulations and sponsor policies; assists in study feasibility, protocol reviews, investigator meetings, regulatory submissions (IRB and others), prepares study materials and regulatory binders, trains study personnel, collects and manages study documents, assists with recruitment strategies and informed consent processes, screens subjects for eligibility, coordinates participant visits and specimen collection, records data and completes Case Report Forms, maintains study timelines and inventory, and communicates with sponsor and participants.