Clinical Research Associate I - Heart Institute - Gupta Team

Grow your career at Cedars-Sinai!

• Cedars-Sinai Medical Center has been named to the Honor Roll in U.S.
• News & World Report’s “Best Hospitals 2025-2026” rankings [https://www.cedars-sinai.org/newsroom/cedars-sinai-ranks-among-top-us-hospitals-for-10th-consecutive-year/].
• When you join our team, you’ll have access to groundbreaking biomedical research facilities and world-class medical education programs.
• We take pride in hiring exceptional, dedicated professionals who are passionate about advancing healthcare.
• Our physicians, nurses, and staff reflect the culturally and ethnically diverse communities we serve and are united by a shared commitment to excellence.
• Together, we foster a dynamic, inclusive environment that drives innovation and supports the gold standard of patient care.

Are you ready to be a part of breakthrough research?

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.

What will you be doing in this role?

• 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.