Clinical Research Coordinator I

Administer clinical tests and questionnaires as part of clinical research protocols (testing visual acuity, stereoacuity, tear collection, electroretinograms, imaging of retina). Data entry for clinical study protocols and preparation of reports. Prepare documents for submission to Research Intake and IRB, including protocols and consent forms, working with faculty, residents, external sponsors and internal departments. Review daily and weekly patient lists across providers, using Cerner to identify potential study participants. Maintain records of eligibility and participation. Work with patients and families to explain the clinical studies, also involved in the consent process and arrange study follow-up. Assist in research coordination to include administrative support schedule coordination, intake and maintaining records/files. Maintain inventory and lab equipment; order lab supplies.