Clinical Research Coordinator I - Trial Operations & Data

The Medical College of Wisconsin, Inc.; United States; On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Healthcare benefits

Onsite facilities

Paid time off

Job summary

The Medical College of Wisconsin, Inc. is seeking an administrative professional to support the clinical research trials program. You will help with day-to-day operations, participant recruitment, consent, and data collection to help meet program goals.

Responsibilities include coordinating protocols, maintaining databases, ensuring IRB and regulatory compliance, and preparing required reports. You will work with study teams and communicate with stakeholders to advance research objectives.

Qualifications

• Associate's degree required; experience may substitute on a 1:1 basis.
• Minimum 1 year of related experience.
• CITI training within 90 days of hire.

Responsibilities

• Recruit, screen, enroll and obtain consent from program participants.
• Coordinate research protocols including appointments and procedures.
• Collect, analyze, and disseminate program data.
• Report program data and progress to stakeholders.
• Assure compliance with IRB and regulatory requirements.
• Assist in IRB documents, reports, and protocol development.
• Collaborate on materials and databases for the program.
• Maintain program timelines and coordinate outreach activities.

Skills

Biology knowledge

Chemistry knowledge

Mathematics

Documentation

Records management

Data analysis

Problem solving

Critical thinking

Resource management

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 help with day-to-day operations, participant recruitment, consent, and data collection to help meet program goals.

Responsibilities include coordinating protocols, maintaining databases, ensuring IRB and regulatory compliance, and preparing required reports. You will work with study teams and communicate with stakeholders to advance research objectives.