Clinical Research Associate I - Urology

Job Description When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. With a team focused on effective pain management and quick recovery, Cedars-Sinai has been ranked as the No. 1 hospital in Southern California for Orthopaedics by U.S. News & World Report. Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. The CRAI evaluates and abstracts research data and ensures compliance with protocol and research objectives. This role is responsible for completing case report forms (CRFs) and entering clinical research data, as well as providing limited contact with research participants as needed for study and assists with study/long term follow-up research participants only. Primary Duties & Responsibilities: u2022Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study. u2022Evaluates and abstracts clinical research data from source documents. u2022Ensures compliance with protocol and overall clinical research objectives. u2022Completes Case Report Forms (CRFs). u2022Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors. u2022Provides supervised patient contact or patient contact for long term follow-up patients only. u2022Assists 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. u2022Assists with clinical trial budgets. u2022Assists with patient research billing. u2022Schedules patients for research visits and research procedures. u2022Responsible for sample preparation and shipping and maintenance of study supplies and kits. u2022Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. u2022Maintains research practices using Good Clinical Practice (GCP) guidelines. u2022Maintains strict patient confidentiality according to HIPAA regulations and applicable law. u2022Participates in required training and education programs Qualifications Educational Requirements: High School Diploma/GED Bachelors degree in science or related degree preferred Experience: 1-year clinical research related experience preferred Physical Demands: Able to perform moderate lifting. Able to sit, stand and walk for prolonged periods of time. Able to read papers and online documents. Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions. Understanding ofu200b general clinical research objectives. Clinical research experience, preferred Req ID : 13483 Working Title : Clinical Research Associate I - Urology Department : Urology Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $19.50 - $32.86Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

Created: 2025-11-15