Clinical Research Coordinator II - Pulmonary Research Program/Lung Institute

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    "ExternalDescriptionStr": "<p><strong>Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!</strong></p>\n<p>Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world.</p>\n<p>As a Clinical Research Coordinator II, you will work independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The incumbent will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. The CRC II member will be responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The incumbent will present information at research staff meetings, may plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. This position ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).</p>\n<p><strong>Primary Duties and Responsibilities:</strong></p>\n<ul>\n <li>Schedules patients for research visits and procedures.</li>\n <li>In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.</li>\n <li>Maintains accurate source documents related to all research procedures.</li>\n <li>Schedules and participates in monitoring and auditing activities.</li>\n <li>Notifies direct supervisor about concerns regarding data quality and study conduct.</li>\n <li>Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.</li>\n <li>May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.</li>\n <li>Maintains research practices using Good Clinical Practice (GCP) guidelines.</li>\n <li>Maintains strict patient confidentiality according to HIPAA regulations and applicable law.</li>\n <li>May coordinate training and education of other personnel.</li>\n <li>May participate in centralized activities such as auditing, Standard Operating Procedure development, etc.</li>\n <li>May identify quality and performance improvement opportunities and collaborate with staff in the development of action plans to improve quality.</li>\n <li>May identify new research opportunities and present to investigators</li>\n <li>Participates in required training and education programs.</li>\n</ul>",
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