Research Nurse Coordinator II - Cancer Clinical Trials Office

Make a difference every single day 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 passion and dedication pulses through Cedars-Sinai, and it’s just one of the many reasons we’ve achieved our fifth-consecutive Magnet designation for nursing excellence. From working with a team of world-class healthcare professionals to using groundbreaking facilities, you’ll have everything you need to do something incredible—for yourself, and for others. Join us, and discover why U.S. News & World Report has named us one of America’s Best Hospitals We encourage you to look at our nursing opportunities at the Samuel Oschin Comprehensive Cancer Institute. We have an immediate opening for a Research Nurse Coordinator II. You will provide educational services to research participants and their family members regarding study participation, participant's current clinical condition, and or disease process. In this role, you will assess and document adverse events as reported by research participants. You will also work closely with the Principal Investigators (PI) to document reports and progress. Additionally, you will record research data where assessed or reported by patient, such as their symptoms of treatment. As a key member of our research team, you will participate in the query and analysis of research data. Responsible for clinical study activities, coordination, adherence to protocols and serves as a liaison between study participants, Principal Investigator (PI), and other research staff. You will have general oversight of research portfolio as it pertains to the clinical coordination of the studies. Collaborates with the team to create and communicate a plan of care that allows for safe and effective collection of clinical research data. You will facilitate and deliver the education of the interdisciplinary team on study requirements You will coordinate research participant study visits and triage study participants by phone and provides clinical information to the study participants. You will recruit study participants and/or lead recruitment activities. You will complete and document study participant enrollment, assessment/reassessment, education, and follow-up activities as well as coordinate study participant interventions as required and/or has oversight of the research activity. Prepare data spreadsheets for PI and/or department and update investigation binders and complete Case Report Forms. You may prepare IRB submissions, assist with data compilation, assist with grant proposals, publication preparation, and presentations. You may oversee grant activities post award through closure including, monitoring budgets, compliance, and progress reports. Jobs-Indeed Requirements: Associate of Science in Nursing (ASN)/College Diploma in Nursing, required. Valid and current California RN license, required. Current Basic Cardiac Life Support (BCLS) certification, required. 3 (three) years Clinical nursing experience required 2 (two) years clinical research experience required Preferred: Bachelor Degree in Nursing or Health Science preferred. Are you seeking an opportunity to demonstrate your positive interpersonal skills and high degree of respect for patients, physicians, and coworkers? Would you like to put your outstanding people skills to work in an environment dedicated to helping others? We would love to hear from you jobs Jobs Working Title: Research Nurse Coordinator II - Cancer Clinical Trials Office Department: CS Cancer Integration & Ops Business Entity: Clinical & Support Services Job Category: Nursing Job Specialty: Research (RN) Position Type: Full-time Shift Length: 8 hour shift Shift Type: Day