Clinical Research Coordinator I: Enroll, Schedule & Track

The Medical College of Wisconsin, Inc.; Milwaukee (WI); On-site; USD 42,000 - 56,000; Full time

Benefits offered by this job

Health coverage

403B retirement

Paid time off

Tuition reimbursement

Parental leave

EFAP

Pet insurance

Onsite fitness facility

Discount programs

Job summary

The Medical College of Wisconsin, Inc. is seeking an administrative professional to support the clinical research trials program. You will perform day-to-day tasks, help with study coordination, and facilitate the program's goals.

Responsibilities include participant recruitment, protocol coordination, data collection and reporting, IRB compliance, and materials development. A 1-year minimum experience and an Associate's degree are required, with CITI training within 90 days of hire.

Qualifications

• Minimum required education: Associate's Degree or equivalent.
• Minimum 1 year of experience in clinical research or related admin work.
• CITI training within 90 days of hire.

Responsibilities

• Recruit, screen, enroll, and consent participants; coordinate training.
• Coordinate research protocols, appointments, and collaborate with other departments.
• Collect, analyze, and report program data to stakeholders.
• Identify problems in procedures and communicate with investigators.
• Ensure IRB and regulatory compliance.
• Assist in IRB document prep and protocol writing.
• Develop program materials and reports.
• Maintain databases/files with the Principal Investigator.
• Maintain program timeline and deadlines.
• Coordinate outreach with community organizations.
• Other duties as assigned.

Skills

Biology

Chemistry

Mathematics

Documentation

Records management

Data analysis

Problem solving

Writing skills

Education

Associate's Degree

Job description

The Medical College of Wisconsin, Inc. is seeking an administrative professional to support the clinical research trials program. You will perform day-to-day tasks, help with study coordination, and facilitate the program's goals.

Responsibilities include participant recruitment, protocol coordination, data collection and reporting, IRB compliance, and materials development. A 1-year minimum experience and an Associate's degree are required, with CITI training within 90 days of hire.