Senior Research Program Coordinator

I maintain a good working knowledge of all assigned protocols and reporting requirements on complex clinical studies which require being responsible for submission, verification, and maintenance of protocol specific information. I maintain a regulatory binder for each assigned protocol so that I can prepare and submit annual renewal requests, amendments, and adverse event reports with clinical input according to IRB and Sponsor requirements, while adhering to all protocol requirements to ensure the validity of the clinical research data. I verify patient eligibility for studies by comparing patient history and clinical laboratory results with protocol requirements and maintain a research chart for each patient by collecting and entering complications of clinical data while ensuring accuracy and timeliness so that information may be used by the physician in treatment planning, presentations, and publication. I schedule patient appointments, tests, and follow up visits at the appropriate time in the treatment cycle to ensure completion of protocol requirements which a variety of different departments. I handle patient screening, recruitment, and consenting and perform interviews, complete structured tests, and collect pertinent data with potential/active research participants.