The Clinical Research Coordinator III at the Smidt Heart Institute works alongside physician-scientists to manage clinical research portfolios and ensure compliance with regulatory standards. This role involves coordinating studies, overseeing research staff, and striving to grow participant enrollment while maintaining high standards for data collection and participant confidentiality. The position requires significant clinical research experience and includes responsibilities such as budgeting, training personnel, and identifying new research opportunities.
The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.
Join our team and use your skill with an organization known nationally for excellence in research!
Job Summary:
Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world.
As a Clinical Research Coordinator III, you will work independently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. This position is responsible for the oversight of all studies with the group and the assignment of studies to clinical research personnel within the group, and supervision of research staff. The incumbent plans and coordinates strategies for growing research participant enrollment, improving efficiency, training of personnel, and identifying new research opportunities. The CRC III member ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
Primary Duties and Responsibilities:
Education:
Licenses/Certifications:
ACRP/SOCRA (or equivalent) certification, preferred.
Experience:
5 years of clinical research experience, required.
Physical Demands:
Clinical Research, Clinical Trials, Patient Enrollment, FDA Compliance, Data Collection, Research Coordinator, Heart Disease Research, Investigational Studies, Good Clinical Practice, Health Care Innovation
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