Senior Clinical Research Coordinator — MOM Study Lead

Washington University in St. Louis; United States; On-site; USD 58,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Tuition assistance

Metro transit U-Pass

Caregiver leave

Job summary

Washington University in St. Louis is seeking a Clinical Research Coordinator to oversee a complex observational MOM study in Saint Louis, MO. You will recruit participants, obtain informed consent, conduct visits in hospital and homes, and ensure protocol and IRB/IACUC compliance.

The role requires hands-on data entry, REDCap/Excel/EPIC experience, and supervisory duties for clinical staff, with travel as needed. Competitive university benefits accompany this position.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• BLS certification must be obtained within one month of hire date.
• Optional SOCRA/ACRP certification based on department needs.
• License to drive and travel to study locations may be required.

Responsibilities

• Coordinate and oversee complex clinical research studies and ensure regulatory compliance.
• Serve as liaison to PI; develop plans, assist with amendments and manuscript prep.
• Train staff and supervise study personnel; monitor progress and data quality.
• Explain study purpose, obtain informed consent, and conduct visits at hospital or participant homes.
• Enter data, assist with lab procedures, and perform data analyses under supervision.

Skills

Clinical Research Management

Clinical Study Protocols

Database Management

Research Projects

Spreadsheet Analysis

SAS

Supervision

Education

Bachelor’s degree

Master’s degree

Tools

REDCap

Excel

EPIC

Job description

Washington University in St. Louis is seeking a Clinical Research Coordinator to oversee a complex observational MOM study in Saint Louis, MO. You will recruit participants, obtain informed consent, conduct visits in hospital and homes, and ensure protocol and IRB/IACUC compliance.

The role requires hands-on data entry, REDCap/Excel/EPIC experience, and supervisory duties for clinical staff, with travel as needed. Competitive university benefits accompany this position.