Pediatric Clinical Research Coordinator I — Critical Care

Washington University in St. Louis; St. Louis (MO); On-site; USD 33,000 - 48,000; Part time

Job summary

Washington University in St. Louis is seeking a Clinical Research Coordinator I for a part-time role (0.5 FTE) to support day-to-day coordination of an ECMO and HD-DOT study in critically ill pediatric participants.

The role involves liaising with the school, sponsoring agencies, and families, and ensuring study compliance across all phases of the protocol. Responsibilities include participant screening, enrollment, obtaining informed consent, data collection, and coordinating with investigators

Qualifications

• Bachelor's degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support certification must be obtained within one month of hire date.
• Clinical Research Coordinator I supports day-to-day coordination of a study involving ECMO and HD-DOT.

Responsibilities

• Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and regulatory requirements; establishes record-keeping systems; analyzes adverse events; informs physicians as needed; coordinates with funding agencies.
• Screens potential participants, recruits and enrolls study participants; determines eligibility; develops informed consent packets; explains procedures to address concerns.
• Ensures timely completion of enrollment documentation and secure storage of forms.
• Ensures timely and accurate collection of clinical data under protocols.
• Performs other duties as assigned.

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 Clinical Research Coordinator I for a part-time role (0.5 FTE) to support day-to-day coordination of an ECMO and HD-DOT study in critically ill pediatric participants.

The role involves liaising with the school, sponsoring agencies, and families, and ensuring study compliance across all phases of the protocol. Responsibilities include participant screening, enrollment, obtaining informed consent, data collection, and coordinating with investigators