We are seeking highly qualified Clinical Research Coordinators I, II, and III, to join our world-renowned organization!
What you do makes a difference, and you have to decide what kind of difference you want to make!
With more than 100 research laboratories and excellent opportunities for growth and development, Cedars-Sinai offers our researchers and scientists unparalleled access to cutting-edge technologies, facilities, and resources for conducting research related to an impressive range of diseases and disorders, from cancer, cardiology, and digestive diseases, to genetics, genomics, neurosciences, and women’s health. Through the power of clinical trials, the researchers at Cedars-Sinai discover new opportunities for advancement in research. To learn more, please visit: Academics & Research at Cedars-Sinai.
Clinical Research Coordinators (CRC) work independently to provide study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Typically, you will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. In addition, Clinical Research Coordinators are responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information, while ensuring compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). In this role, you will have an opportunity to present study information at regular research staff meetings.
Role-Specific Qualifications:
CRC I
- Education: Bachelor’s Degree in Science, Sociology or related degree
- Experience: 2 years of directly related experience
CRC II
- Education: Bachelor’s Degree in Science, Sociology or related degree
- Experience: 4 years of directly related experience
- May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities.
CRC III
- Education: Bachelor’s Degree in Science, Sociology or related degree
- Experience: 5 years of directly related experience
- Responsible for oversight of all studies with the group and the assignment of studies to clinical research personnel within the group, and supervision of research staff.
- Plans and coordinates strategies for increasing patient enrollment, improving efficiency, training of personnel, and identifying new research opportunities.
Remember when you said you wanted to make a difference? Here’s your chance. Apply now and with your support, we can change the future of healthcare.
Working Title: Clinical Research Coordinator
Department: Heart Institute
Business Entity: Academic / Research
Job Category: Academic/Research
Job Specialty: Research Studies/Clinical Trials
Position Type: Full-time
Shift Length: 8 hour shift
Base Pay:$23.39 – $39.76