Clinical Research Coordinator I - Protocols & Compliance

UNKNOWN; United States; On-site; USD 33,000 - 49,000; Full time

Benefits offered by this job

Vacation days

Health insurance

Metro U-Pass

403(b) Retirement Savings

Wellness programs

Caregiver leave

Job summary

Washington University in St. Louis seeks a Clinical Research Coordinator to assist investigators across basic to moderately complex studies, coordinating multiple protocols while liaising with faculty, sponsors, community, and participants.

You will manage all study phases to ensure protocol compliance and timely delivery. The role involves participant recruitment, informed consent, administering tests, data recording, and reporting adverse events, with a 40-hour work week and a salary range of

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.
• Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirement).
• No specific work experience is required for this position.

Responsibilities

• Implements and manages all phases of study/protocol; ensures protocol compliance.
• Recruits and enrolls study participants and assesses eligibility.
• Analyzes, reports adverse events and coordinates with physicians as needed.
• Collects clinical data, prepares progress reports and communicates findings.

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 assist investigators across basic to moderately complex studies, coordinating multiple protocols while liaising with faculty, sponsors, community, and participants.

You will manage all study phases to ensure protocol compliance and timely delivery. The role involves participant recruitment, informed consent, administering tests, data recording, and reporting adverse events, with a 40-hour work week and a salary range of