Pediatric Clinical Research Coordinator

Scottish Rite for Children

Dallas (TX)

On-site

USD 55,000 - 75,000

Full time

14 days+
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Job summary

Scottish Rite for Children is seeking a Research Coordinator in Dallas, TX, to support pediatric research initiatives. The role involves coordinating studies, maintaining regulatory documentation, and ensuring GCP compliance.

You will manage REDCap data, assist with study design, and help investigators with submissions for IRB and publications. The position requires a Bachelor’s degree and experience in clinical research; CCRP is preferred.

Qualifications

  • Bachelor's degree required.
  • Clinical research and regulatory experience preferred (3+ years).
  • CCRP certification preferred.
  • Experience with REDCap or other electronic data capture systems preferred.

Responsibilities

  • Collaborate with staff in research divisions and clinical departments to obtain information and support for research.
  • Organize and lead project meetings, communicate study updates, and provide regular reports to Principal Investigators.
  • Prepare regulatory documents, consent forms, and submissions for IRB and other agencies.
  • Coordinate study visits, procedures, and data collection per protocol.
  • Maintain regulatory binders, source documents, and audit readiness for inspections.
  • Screen, recruit, consent, and enroll participants while ensuring protocol compliance.

Skills

Clinical research
Regulatory compliance
Project coordination
REDCap data capture
Epic EMR
Microsoft Office

Education

Bachelor's degree in a related field

Tools

REDCap
Epic
Microsoft Office

Job description

Scottish Rite for Children is seeking a Research Coordinator in Dallas, TX, to support pediatric research initiatives. The role involves coordinating studies, maintaining regulatory documentation, and ensuring GCP compliance.

You will manage REDCap data, assist with study design, and help investigators with submissions for IRB and publications. The position requires a Bachelor’s degree and experience in clinical research; CCRP is preferred.

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