Clinical Research Coordinator II: Trials, Data & Compliance

Medical College of Wisconsin; West Bend (WI); On-site; USD 52,000 - 68,000; Full time

Benefits offered by this job

Healthcare benefits

Retirement plan

Paid time off

Job summary

Medical College of Wisconsin is seeking a Clinical Research Program Coordinator to handle day-to-day administrative tasks for clinical research trial programs and to support the team in achieving program objectives.

You will recruit and consent participants, coordinate protocols and appointments, manage data and budgets, ensure IRB compliance, and contribute to the development of educational and marketing materials. A Bachelor's degree and at least two years of experience are required.

Qualifications

• Bachelor's degree required.
• Minimum of 2 years' experience in clinical research or a related field.
• CITI training completed within 90 days of hire.

Responsibilities

• Recruit, screen, enroll, and consent participants.
• Coordinate research protocols and appointments.
• Collect, analyze, and disseminate data and manage databases.
• Ensure compliance with IRB and regulatory requirements.
• Prepare IRB documents and protocol evaluations with investigators.
• Monitor program budget and resources.

Skills

Biology knowledge

Chemistry knowledge

Mathematics

Documentation

Records management

Data analysis

Critical thinking

Writing skills

Education

Bachelor's degree

Job description

Medical College of Wisconsin is seeking a Clinical Research Program Coordinator to handle day-to-day administrative tasks for clinical research trial programs and to support the team in achieving program objectives.

You will recruit and consent participants, coordinate protocols and appointments, manage data and budgets, ensure IRB compliance, and contribute to the development of educational and marketing materials. A Bachelor's degree and at least two years of experience are required.