Clinical Research Coordinator I — Trials, Data & Compliance

mcw; Milwaukee (WI); On-site; USD 45,000 - 60,000; Full time

Benefits offered by this job

Health coverage

Flexible spending

403B retirement

Vacation & holidays

Tuition reimbursement

Parental leave

EFAP

Pet insurance

On-site gym

Discounts

Job summary

MCW seeks an administrative coordinator to support day-to-day operations of our clinical trials program in Milwaukee. You will work with Principal Investigators to ensure protocol compliance and data integrity across trials at CHW and affiliated sites.

The role requires coordinating with CTO leads, screening and enrolling participants, and maintaining regulatory training (CITI/GCP) while ensuring HIPAA/GCP compliance and diligent data management.

Qualifications

• Associate degree required or equivalent experience.
• CITI and GCP training within 90 days of hire.
• Equivalent experience may substitute for education.

Responsibilities

• Coordinate trials with Principal Investigators and CHW, ensuring proper conduct.
• Support CTO leads daily and manage priorities.
• Screen, recruit, enroll and obtain consent from participants.
• Coordinate research protocols and appointments with other departments.

Skills

Biology

Chemistry

Mathematics

Documentation

Records management

Education

Associate's Degree

Tools

EPIC EMR

OnCore

Job description

MCW seeks an administrative coordinator to support day-to-day operations of our clinical trials program in Milwaukee. You will work with Principal Investigators to ensure protocol compliance and data integrity across trials at CHW and affiliated sites.

The role requires coordinating with CTO leads, screening and enrolling participants, and maintaining regulatory training (CITI/GCP) while ensuring HIPAA/GCP compliance and diligent data management.