Pediatric Clinical Research Coordinator II – Evening

Children’s Hospital of Orange County

United States

On-site

USD 88,700,000 - 146,224,000

Full time

8 days ago
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Job summary

CHOC in Orange, California is seeking a Clinical Research Coordinator II to provide multi-project coordination support for pediatric clinical research efforts. The role involves feasibility assessment, IRB preparation, participant identification, data collection, and record keeping with strict regulatory adherence.

With minimal supervision, you will ensure timely study documentation, quality audits, and effective cross-team communication while supporting compliance with ICH-GCP guidelines and

Qualifications

  • Minimum three years of clinical research coordination experience.
  • Associate degree or equivalent; Bachelor’s preferred.
  • Basic knowledge of Microsoft Office programs (Word, Excel, PowerPoint).
  • Working knowledge of human subjects’ regulatory requirements (ICH-GCP).

Responsibilities

  • Provide coordinator support to multiple human subjects research projects.
  • Assess feasibility of clinical protocols and prepare IRB submissions.
  • Identify potential study participants and coordinate data/specimen collection.
  • Maintain study records accurately and on time; participate in QA audits.
  • Archive records per policy and manage study materials and supplies.

Skills

Clinical research coordination
IRB submissions
ICH-GCP knowledge
Data collection
Regulatory compliance
Communication
Microsoft Office

Education

Associate degree or equivalent experience
Bachelor’s degree (preferred)

Tools

Cerner or EMR

Job description

CHOC in Orange, California is seeking a Clinical Research Coordinator II to provide multi-project coordination support for pediatric clinical research efforts. The role involves feasibility assessment, IRB preparation, participant identification, data collection, and record keeping with strict regulatory adherence.

With minimal supervision, you will ensure timely study documentation, quality audits, and effective cross-team communication while supporting compliance with ICH-GCP guidelines and

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