Clinical Research Coordinator (RN):… at Hoag Health… · 1 Hoag Dr

Summary: Hoag Health System is a nonprofit regional health care delivery network in Orange County, California, and they are seeking a Clinical Research Coordinator RN. The CRC-RN is responsible for all aspects of clinical research activities, including coordination of FDA regulated research and ensuring the smooth process of clinical studies from planning to completion. Responsibilities: - Responsible for all aspects of clinical research activities and works in close cooperation with study physicians - Provides support, coordination and leadership for FDA regulated research including drug/device/biologic studies that may involve industry-sponsored Phase I, II, III and IV clinical trials, government funded clinical research and investigator initiated clinical research - Ensures smooth, accurate process of clinical studies from the planning and approval stages through study completion and post-study closure - Reports to the Director of Clinical Research - Involved in all aspects of research studies from protocol review, preparation and administration of the informed consent, study submission to the Institutional Review Board, subject recruitment, accurate data collection and completion of case report forms (CRFs), adverse event reporting, scheduled subject follow-up, and maintenance of regulatory binders - Discusses research study with potential study subjects and answers any questions (may refer questions to Principal Investigator when appropriate) while obtaining informed consent as well as assisting in scheduling follow-up visits for enrolled subjects - Assists in developing a detailed cost analysis, study budget preparation, and tracking/distribution of study funds - Responsible for submitting case report forms and other data to the Sponsor as necessary, and assists with monitoring, auditing and close-out visits - Maintains knowledge of best practice and standards for Good Clinical Practices, protection of human subjects in research practices, and FDA regulatory guidelines regarding clinical research Required Qualifications: - One year of Clinical Research Coordinator experience or at least three years of experience in the specific medical specialty of the position - Patient coordination experience in complex clinical trial setting required - Medical terminology required - Working knowledge of FDA, NIH and OHRP regulatory requirements and ICH GCP guidelines - Understanding of clinical trial methodologies and experience filing Institutional Review Board documents - Current licensure in good standing as a Registered Nurse in the State of California Preferred Qualifications: - Bachelor of Science in Nursing (BSN) preferred - Familiar with the medical area of neurosciences particularly in the areas of stroke, epilepsy, movement disorders and cognitive disease preferred - Holds current Certified Clinical Research Coordinator certificate (ACRP or SoCRA), or complete within two years of hire - Maintain CPR, certifications (BLS, ACLS, NALS, PALS, E.P., etc.) as applicable per hospital policy Required Skills: Clinical Research Coordination, Patient Coordination, Medical Terminology, FDA Regulatory Requirements, NIH Regulatory Requirements, OHRP Regulatory Requirements, ICH GCP Guidelines, Clinical Trial Methodologies, Institutional Review Board Documentation, Registered Nurse License, Certified Clinical Research Coordinator, CPR Certification, BLS Certification, ACLS Certification, NALS Certification, PALS Certification