Pediatric Endocrinology Clinical Research Coordinator

Washington University in St. Louis

United States

On-site

USD 49,000 - 74,000

Full time

3 days ago
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Benefits offered by this job

Vacation & sick time
Health insurance
Metro U-Pass for eligible employees
Retirement Savings Plan (403(b))

Job summary

Washington University in St. Louis is seeking a motivated Clinical Research Coordinator to oversee basic to moderately complex studies, liaising with the school, sponsor agencies, and participants.

This role involves coordinating visits, data entry, regulatory compliance, and communication with families and investigators. You will work with pediatric participants and their families, manage enrollment and screening, and ensure timely completion of all study requirements, including data management

Qualifications

  • Bachelor’s degree required or equivalent combination of education and experience.
  • Basic Life Support certification is required or expected (AHA/BLS).
  • No specific prior work experience is required for this role.
  • Skills are not listed as a separate category beyond clinical research competencies.

Responsibilities

  • Coordinate all phases of clinical research studies and ensure protocol compliance.
  • Maintain records and manage regulatory documents and sponsor requirements.
  • Screen, enroll and follow up with participants and families as applicable.
  • Schedule study visits, collect data, and manage data entry and tracking.
  • Monitor progress, adverse events, and protocol deviations; communicate with investigators.

Skills

Clinical Research
Study Protocols
Communication
Computer Systems
Interpersonal Communication
Organizing
Research Support

Education

Bachelor’s degree

Job description

Washington University in St. Louis is seeking a motivated Clinical Research Coordinator to oversee basic to moderately complex studies, liaising with the school, sponsor agencies, and participants.

This role involves coordinating visits, data entry, regulatory compliance, and communication with families and investigators. You will work with pediatric participants and their families, manage enrollment and screening, and ensure timely completion of all study requirements, including data management

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