Clinical Research Coordinator I - Guerin… at Cedars-Sinai · 6500…

Summary: Cedars-Sinai is a leader in providing high-quality healthcare and is seeking a Clinical Research Coordinator I for their Pediatric NICU. The role involves independent study coordination, patient screening for protocol eligibility, and ensuring compliance with federal and local regulations. Responsibilities: - Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process - Schedules patients for research visits and procedures - 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 - Maintains accurate source documents related to all research procedures - Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries - Schedules and participates in monitoring and auditing activities - Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings - Notifies direct supervisor about concerns regarding data quality and study conduct - 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 - May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation - 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 - Participates in required training and education programs Required Qualifications: - High School Diploma/GED required - One (1) year of clinical research related experience required Preferred Qualifications: - Bachelor's Degree in Science, Sociology or related degree preferred - SOCRA or ACRP certification preferred upon hire - Prior interventional clinical trial & pediatric NICU clinical research experience is desired Required Skills: Clinical Research Coordination, Patient Screening for Protocol Eligibility, Informed Consent Process, Case Report Forms (CRFs) Documentation, Data Collection and Entry, Regulatory Compliance with FDA and IRB, Clinical Practice (GCP) Guidelines, HIPAA Regulations Compliance, SOCRA Certification, ACRP Certification, Interventional Clinical Trials, Pediatric NICU Clinical Research