Clinical Research Coordinator I
4 weeks ago
Cedars-Sinai is seeking a Clinical Research Coordinator I to join our Pulmonary Research Program/Lung Institute. The successful candidate will work independently to provide study coordination, screen patients for protocol eligibility, and present non-medical trial concepts and details. This role is responsible for accurate and timely source documents, data collection, documentation, entry, and reporting, including timely response to sponsor queries.
Key Responsibilities:
* Coordinate clinical trials, including scheduling patients for research visits and procedures
* Document thoroughly on Case Report Forms (CRFs) and maintain accurate source documents related to all research procedures
* Notify direct supervisor about concerns regarding data quality and study conduct
* Work closely with regulatory coordinators 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
* Perform other regulatory/IRB duties, budgeting duties, and assist with patient research billing and reconciliation
* Maintain research practices using Good Clinical Practice (GCP) guidelines
Requirements:
* Bachelor's degree, preferred
* 1 year of clinical research experience, required
About Cedars-Sinai:
Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine, and research. We are committed to the community through programs that improve the health of our most vulnerable residents. As one of the largest nonprofit academic medical centers in the nation, we offer a fast-paced environment that provides the highest level of care to people in the Los Angeles area who need our care the most.
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