Clinical Research Coordinator I

This position will coordinate multiple clinical trial studies independently. Will manage patients enrolled in clinical studies and guide them through study visits while overseeing all aspects of the clinical trial process which includes: participate in subject identification and recruitment; oversee the consent process; gather, transcribe, and enter study data into sponsor databases; manage and handle laboratory supplies and data; gather and handle biospecimens; create source documents to collect study data; ensure quality control, compile reports for regulatory compliance and maintenance while complying with clinical trial study requirements. Will also troubleshoot to avoid protocol deviations. Will complete all training requirements for each study, attend study meetings as necessary, and participate in monitoring visits and audits. Will act as the regulatory backup to the Senior CRA, which would require submission of IRB applications/renewals and study startup coordination.