Cedars - Sinai

As a Clinical Research Associate I, you will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study.. Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine, and research.. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching, and community service.. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients.. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals.

clinical research associate i

﻿<div><h5><p>Job Description</p></h5><p>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.</p><p>We invite you to consider this phenomenal opportunity!</p><p>Dr. Teryl Nuckols studies the quality/safety of healthcare: how do you measure it, how do you improve it, and what does it cost? She is active in mentoring junior investigators in health services research both at the junior faculty and research stages. Dr. Nuckols is PI of an AHRQ-funded RCT testing a strategy for engaging nurses in reporting medication safety events and developing prevention strategies.</p><p>As a Clinical Research Associate I, you will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role evaluates and abstracts research data, and ensures compliance with protocol and research objectives. Position is responsible for completing case report forms (CRFs), entering clinical research data, and assisting with regulatory submissions to the Institutional Review Board (IRB). The CRA I may have limited contact with research participants as needed for study and assists with study budget and research participant billing. This role follows all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.</p><h5><p>Primary Job Duties and Responsibilities:</p></h5><ol><li>Evaluates and abstracts clinical research data from source documents.</li><li>Ensures compliance with protocol and overall clinical research objectives.</li><li>Completes Case Report Forms (CRFs).</li><li>Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.</li><li>Provides supervised patient contact or patient contact for long term follow-up patients only.</li><li>Assists 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.</li><li>Assists with clinical trial budgets.</li><li>Assists with patient research billing.</li><li>Schedules patients for research visits and research procedures.</li><li>Responsible for sample preparation and shipping and maintenance of study supplies and kits.</li><li>Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.</li><li>Maintains research practices using Good Clinical Practice (GCP) guidelines.</li><li>Maintains strict patient confidentiality according to HIPAA regulations and applicable law.</li><li>Participates in required training and education programs.</li></ol><h5><p>Qualifications</p></h5><ul><li>Education:<ul><li>High School Diploma/G.E.D., required.</li><li>Bachelor's degree in Science, Sociology, or related degree, preferred.</li></ul></li><li>Licenses/Certifications:<ul><li>ACRP/SoCRA (or equivalent) certification is preferred.</li></ul></li><li>Experience:<ul><li>Clinical Research experience is highly preferred.</li><li>Understanding of general research objectives.</li></ul></li></ul><h5><p>About Us</p></h5><p>Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine, and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching, and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.</p><h5><p>About the Team</p></h5><p>Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses, and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in Los Angeles who need our care the most.</p><p>Req ID: 2092</p><p>Working Title: Clinical Research Associate I - General Internal Medicine</p><p>Department: Research - General Medicine</p><p>Business Entity: Cedars-Sinai Medical Center</p><p>Job Category: Academic / Research</p><p>Job Specialty: Research Studies/ Clin Trial</p><p>Overtime Status: NONEXEMPT</p><p>Primary Shift: Day</p><p>Shift Duration: 8 hours</p><p>Base Pay: $19.50 - $29.87</p></div><h3>J-18808-Ljbffr</h3>

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