NICU Clinical Research Coordinator I

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 U-Pass

Retirement plan (403b)

Job summary

Washington University in St. Louis seeks a Clinical Research Coordinator to support newborn NICU studies at Saint Louis Children’s Hospital.

You will coordinate studies, manage regulatory requirements, and liaise with investigators, sponsors, and participants to ensure protocol compliance and timely data collection. The role involves hands-on patient interaction, strong organizational skills, and the ability to multi-task across studies.

Qualifications

• Bachelor’s degree or equivalent combination of education and experience.
• Basic Life Support certification from American Heart Association or American Red Cross.

Responsibilities

• Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and regulatory requirements; maintains records; assesses participant progress; reports adverse events; coordinates with funding agencies.
• Recruits and enrolls participants; determines eligibility; obtains informed consent; explains procedures and treatment plans; administers tests and ensures timely completion of assessments.
• Ensures timely completion of all protocol requirements (assessments, lab testing, procedures, treatments); analyzes data and prepares reports.
• Collects clinical data under clinical research 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 seeks a Clinical Research Coordinator to support newborn NICU studies at Saint Louis Children’s Hospital.

You will coordinate studies, manage regulatory requirements, and liaise with investigators, sponsors, and participants to ensure protocol compliance and timely data collection. The role involves hands-on patient interaction, strong organizational skills, and the ability to multi-task across studies.