Clinical Research Coordinator I - Study Liaison & Data

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

Benefits offered by this job

Up to 22 days of vacation

Competitive health insurance packages

Metro transit U-Pass

Job summary

Washington University in St. Louis is seeking a Clinical Research Study Coordinator to assist investigators across basic to moderately complex studies.

The role coordinates multiple studies, liaises with sponsors, and ensures protocol compliance and proper record-keeping. Responsibilities include recruiting participants, obtaining informed consent, managing data, and reporting adverse events while supporting scheduling and regulatory requirements.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support certification is required.

Responsibilities

• Implements and manages all phases of study/protocol and ensures compliance with protocol guidelines and regulatory requirements.
• Recruits and enrolls study participants and confers with participants to obtain informed consent packets.
• Ensures timely completion of protocol requirements including scheduling and data collection; analyzes data and reports trends.
• 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 is seeking a Clinical Research Study Coordinator to assist investigators across basic to moderately complex studies.

The role coordinates multiple studies, liaises with sponsors, and ensures protocol compliance and proper record-keeping. Responsibilities include recruiting participants, obtaining informed consent, managing data, and reporting adverse events while supporting scheduling and regulatory requirements.