Cedars-Sinai
Posted 87 days agoVerified live 9h ago
Clinical Research Data Specialist I - Ouyang Lab
Brief overview
Los Angeles, CAIn-person
$24–$39/hrStated range
1+ yrsMinimum
255 H-1B approvalsDept. of Labor
20 green cardsCertified filings
About the company
Cedars-Sinaicedars-sinai.org
Since its beginning in 1902, Cedars-Sinai has evolved to meet the healthcare needs of one of the most diverse regions in the nation, continually setting new standards for quality and innovation in patient care, research, teaching and community service.
Visa sponsorship history
4 years sponsoring, last filed FY2026
Data powered by U.S. Department of Labor. This does not guarantee sponsorship for this specific role.255H-1B approved
98%approval rate
131new H-1B hires
20PERM certified
$83,792median wage / yr
H-1B Petition ApprovalsVisas USCIS actually granted: the strongest sign the company sponsors.
202373
202477
202593
202612
LCA Certified ApplicationsAn early filing step, not a visa approval: it signals intent, not confirmed sponsorship.
202326
202429
202527
202624
Green Card (PERM) FilingsCertified green card filings: a long-term commitment to international hires.
20234
20242
202513
20261
Top sponsored roles
Postdoctoral ScientistProject ScientistResearch ScientistResearch BioinformaticianResearch Associate
Sponsored employees from
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Job description
Summary
Cedars-Sinai Medical Center is a leading healthcare institution known for its dedication to advancing healthcare through groundbreaking research. The Clinical Research Data Specialist I will manage data for assigned research studies, ensuring accuracy and compliance with federal regulations while designing forms for data collection and producing project reports.
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
Skills
- 1 year of experience in related field
- Bachelor's degree in a relevant field (e.g., life sciences, health sciences) preferred
- 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
Qualifications
Must Haves
- 1 year of experience in related field
Nice to Haves
- Bachelor's degree in a relevant field (e.g., life sciences, health sciences) preferred
- 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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