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Open nowPosted 3 days ago

Clinical Research Data Specialist I - Heart Institute - Ouyang Lab

Cedars-Sinai74 open roles

Where
Los Angeles, CA, United States
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Your applicationOpen nowClinical Research Data Specialist I - Heart Institute - Ouyang LabCedars-Sinai · Los Angeles, CA, United States

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The clock on this job

Early applications get read.

8.2% of postings close within 7 days. Measured by our own scanner across the market. Cedars-Sinai postings stay open a median of 5 days.

Share of postings closed within
  1. 1.9%1 day
  2. 3.8%3 days
  3. 8.2%7 days
  4. 15.2%14 days
  5. 34.2%30 days
This job: posted 3 days ago

Cedars-Sinai median: 5 days open

The posting

Job Description

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. 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 an increasing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.

Dr. Ouyang is a physician-scientist and cardiologist with subspecialty expertise in non-invasive imaging and technical background in programming, statistics, and deep learning. As a statistician by training, he has always been fascinated by how to understand, visualize, and interpret data. With the exponential rise in the amount of data being collected in clinical care, there are huge opportunities to apply the additional data to personalize care and improve diagnosis and treatment of cardiovascular disease. Dr. Ouyang's goal as an investigator is to have expertise in echocardiography and deep learning applied to medical imaging, while leveraging clinically generated data to inform scientific discovery. His previous work has demonstrated the ability of convolutional neural networks to identify systemic human phenotypes that modify cardiovascular risk previously thought to be not apparent on echocardiographic images and precision phenotyping of cardiac function with higher precision than human interpreters. As an advanced cardiac imager and cardiologist, Dr. Ouyang hopes to advance and enhance cardiovascular imaging.

What will you be doing in this role?

The Clinical Research Data Specialist I manages the data for assigned research studies. This will include, designing forms for data collection, clinical data abstraction, processing data, maintaining record systems, and producing project reports for studies. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.

Primary Duties and Responsibilities:

  • Manages and maintains research data to ensure accuracy, integrity, and security of complex, large computerized records systems. This includes performing data searches and other related administrative tasks.
  • Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data.
  • Designs forms for data collection and performs clinical data collection/abstraction.
  • Produces project reports for research studies.
  • Understands regulations, policies, protocols and procedures to control and maintain accurate records.
  • Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
  • Maintains research practices using Good Clinical Practice (GCP) guidelines.
  • Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
  • Participates in required training and education programs.

Qualifications

Education:

  • Bachelor's degree in a relevant field (e.g., life sciences, health sciences) preferred.

Experience:

  • 1 year of experience in related field.
  • Training in biostatistics, epidemiology, statistics, or a related field preferred. Analytical experience using Electronic Health Record (EHR) data, longitudinal data, and advanced clinical statistical models is preferred.
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