Clinical Research Associate I - Heart Institute

CEDARS-SINAI

Costa Mesa, CAFull-timePosted Apr 25, 2026

Behavioral Health Market Context

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Benefits

Shift Length: 8 hourSalary Range: $24.00 - $32.86

Qualifications

  • High School Diploma is required

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
  • Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study
  • Evaluates and abstracts clinical research data from source documents
  • Ensures compliance with protocol and overall clinical research objectives
  • Completes Case Report Forms (CRFs)
  • Enters clinical research data into Electronic Data Systems (EDCs) that the sponsors provide
  • Provides supervised patient contact or patient contact for long term follow-up patients only
  • Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines
  • Assists with clinical trial budgets
  • Assists with patient research billing
  • Schedules patients for research visits and research procedures
  • Responsible for sample preparation and shipping and maintenance of study supplies and kits
  • 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
  • 17 more items(s)


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