Pediatric Clinical Research Coordinator I (Endocrinology)

Washington University in St. Louis; St. Louis (MO); On-site; USD 49,000 - 74,000; Full time

Benefits offered by this job

Vacation time

Health insurance

Metro transit U-Pass

403(b) Retirement Savings Plan

Wellness programs

4 weeks caregiver leave

Tuition benefits

Job summary

Washington University in St. Louis is seeking a motivated Clinical Research Coordinator to assist investigators across pediatric studies, coordinating multiple research activities and serving as a liaison with the school, sponsors, participants and families.

Key duties include participant screening and enrollment, scheduling study visits, collecting and managing data, maintaining regulatory documentation, and coordinating with clinical teams to ensure protocol compliance and patient safety.

Qualifications

• Bachelor's degree or combination of education and/or experience may substitute for minimum education.
• No specific work experience is required for this position.
• Regulatory knowledge and familiarity with Good Clinical Practice (GCP) and related agencies is beneficial.

Responsibilities

• Implements and manages all phases of clinical research studies and ensures regulatory compliance.
• Recruits and enrolls study participants; screens for eligibility and coordinates informed consent.
• Maintains study materials, databases, and data management procedures; collects and manages data.
• Coordinates visits, laboratory testing, and follow-up activities; communicates with families and clinical staff.

Skills

Clinical Research

Clinical 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 assist investigators across pediatric studies, coordinating multiple research activities and serving as a liaison with the school, sponsors, participants and families.

Key duties include participant screening and enrollment, scheduling study visits, collecting and managing data, maintaining regulatory documentation, and coordinating with clinical teams to ensure protocol compliance and patient safety.