Clinical Research Coordinator I

Clinical Research Coordinator I assists on clinical research studies by recruiting, evaluating, and consenting patients; collecting and organizing patient data; scheduling study visits; and performing clinical tests such as phlebotomy and EKGs. The role includes maintaining study data, assisting with regulatory binders and QA/QC procedures, interviewing subjects, and supporting regulatory submissions. Candidates may have a bachelor’s degree in a related field with a six-month grace period to provide degree equivalency verification; per diem arrangements may apply.