Cardiology Clinical Research Associate I/CPT

VetJobs

Los Angeles (CA)

On-site

USD 34,000 - 46,000

Full time

15 hours ago
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Job summary

Cedars-Sinai's Smidt Heart Institute invites applications for a Clinical Research Associate I/CPT to support noncomplex studies under supervision in Los Angeles. The role involves data collection, participant prescreening, and assisting with regulatory submissions to the IRB while ensuring budget alignment and patient confidentiality.

Ideal candidates have at least a high school diploma, CPT‑phlebotomy certification, and up to one year of clinical research experience.

Qualifications

  • Educational Requirements: High school diploma/GED required
  • Bachelor's degree in Science, Sociology or related degree preferred
  • Licenses: CPT- Phlebotomy Certification license required
  • Experience: 1 year clinical research experience preferred

Responsibilities

  • Assists in coordinating noncomplex research studies
  • Collects and abstracts clinical research data
  • Enters data into Electronic Data Systems (EDCs) provided by sponsors
  • Completes Case Report Forms (CRFs)
  • Assists with prescreening of potential research participants and scheduling visits
  • Supports regulatory submissions to IRB including Adverse Events and Safety Letters
  • Assists with budget and patient research billing
  • Responsible for sample preparation and shipping, and kit maintenance
  • Ensures compliance with GCP and HIPAA regulations
  • Acts as a primary contact for sponsor inquiries when directed

Skills

Data collection
Prescreening
IRB submissions
Budget & billing
GCP compliance
HIPAA compliance

Education

High School diploma or GED
Bachelor's degree in Science or related field
CPT-Phlebotomy certification

Tools

EDCs software

Job description

Cedars-Sinai's Smidt Heart Institute invites applications for a Clinical Research Associate I/CPT to support noncomplex studies under supervision in Los Angeles. The role involves data collection, participant prescreening, and assisting with regulatory submissions to the IRB while ensuring budget alignment and patient confidentiality.

Ideal candidates have at least a high school diploma, CPT‑phlebotomy certification, and up to one year of clinical research experience.

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