Clinical Research Coordinator I

Coordinate clinical research for human subjects studies, including basic science, phase II through IV trials, and IIR studies. Follow guidelines for identifying subject populations, complete forms, and procedures for collecting and summarizing observations and data. Prepare for and participate in study monitor visits, and may perform venous blood draws within the Medical Assistant scope. Coordinate and oversee processing, inventory, and shipping of study specimens, while documenting accurate records of study visits and eCRF completion. Submit sponsor queries within 3–5 business days. Requires a high school education with a bachelor's degree preferred, minimum one year of research experience, CPR certification, and a valid Washington State driver's license.