Clinical Research Coordinator — Participant Enrollment & Data

The Medical College of Wisconsin, Inc.; United States; On-site; USD 52,000 - 68,000; Full time

Benefits offered by this job

Healthcare Coverage (Health, Vision, &

Flexible Spending options

Paid Holidays

Tuition Reimbursement

On campus Fitness Facility

Job summary

The Medical College of Wisconsin is seeking a detail-oriented clinical research administrator to perform day-to-day activities within the trials program. You will support the research team to achieve program goals, recruit participants, coordinate protocols, and manage study data.

Responsibilities include training participants, coordinating appointments, ensuring IRB compliance, preparing documents, and maintaining databases and reports.

Qualifications

• Minimum required education: Associate's Degree.
• Minimum required experience: 1 year.
• Required Certification/Licensure: CITI training within 90 days of hire.

Responsibilities

• Recruit, screen, enroll and obtain consent from program participants.
• Coordinate training for program participants.
• Arrange appointments and procedures, collaborating with other departments and maintaining contact with participants.
• Collect, analyze, and disseminate program data.
• Report program data and progress to stakeholders.
• Ensure compliance with IRB and regulatory requirements.
• Assist in IRB documents and reports.
• Assist in evaluation and writing of research protocols.
• Develop program materials and reports and manage databases and files.
• Maintain program timeline and deadlines for components.
• Coordinate outreach with community organizations.

Skills

Biology knowledge

Chemistry knowledge

Mathematics knowledge

Documentation

Records management

Data analysis

Critical thinking

Writing skills

Education

Associate's degree

Job description

The Medical College of Wisconsin is seeking a detail-oriented clinical research administrator to perform day-to-day activities within the trials program. You will support the research team to achieve program goals, recruit participants, coordinate protocols, and manage study data.

Responsibilities include training participants, coordinating appointments, ensuring IRB compliance, preparing documents, and maintaining databases and reports.