CEDARS-SINAI • Los Angeles, CA 90071 • Posted 2 days ago
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The Clinical Research Associate I at Cedars-Sinai's Smidt Heart Institute works closely with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and implement clinical research studies. This role involves evaluating and abstracting research data, ensuring compliance with protocol and research objectives, completing case report forms, entering clinical research data, assisting with regulatory submissions, and providing limited patient contact as needed. The position requires adherence to all relevant federal, local, FDA, IRB, and HIPAA guidelines and regulations.
About CEDARS-SINAI
Cedars-Sinai is a leading nonprofit hospital in Los Angeles, providing exceptional specialty care across various medical disciplines. They are renowned for their groundbreaking research, cutting-edge treatments, and commitment to redefining patient care standards, offering world-class healthcare services with expertise and compassion.
Grow your career at Cedars-Sinai!
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 niche 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 skills with an organization known nationally for excellence in research!
Key Job Responsibilities:The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.
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