Clinical Research Associate I - Surgery Chair

Clinical Research Associate IThe Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.Works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies.Collects, evaluates and/or abstracts clinical research data. May assist in designing forms for data collection/abstraction. Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.Completes Case Report Forms (CRFs).Assists with prescreening of potential research participants for various clinical trials. Schedules research participants for research visits and research procedures. Provides supervised patient contact or independent patient contact for long term follow-up patients only.Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.Assists with clinical trial budgets and patient research billing.Responsible for sample preparation and shipping and maintenance of study supplies and kits.Ensures compliance with protocol and overall clinical research objectives. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.May serve as one point of contact for external sponsors for select trials. May respond to sponsor inquiries and attend meetings regarding study activity under the direction of supervising staff.QualificationsEducationHigh School Diploma/GED - minimumBachelor's Degree Science, Sociology or related degree. - preferredExperience1 year Clinical research related experience - preferredJob InfoJob Identification 21194Legal Employer Cedars-Sinai Medical CenterDepartment CSMC 8020204 Research - Surgery ChairJob Category Academic / ResearchJob Function Research Studies/ Clin TrialLocations 6500 Wilshire Blvd, Los Angeles, CA, 90048, USOvertime Status NONEXEMPTPrimary Shift 1 DayShift Duration 8 hourMinimum Salary 25.00Maximum Salary 33.51UKG Pay Rule C007Posting Date 10/20/2026, 04:58 PM