Ophthalmology Clinical Research Coordinator II

The Medical College of Wisconsin, Inc.; Milwaukee (WI); Vor Ort; USD 55.000 - 75.000; Vollzeit

Benefits dieser Stelle

Healthcare coverage

403B Retirement Package

Vacation and Paid Holidays

Tuition Reimbursement

Parental Leave

EFAP

Pet Insurance

On campus Fitness Facility

Zusammenfassung

The Medical College of Wisconsin, Inc. seeks a Clinical Research Coordinator II in the Department of Ophthalmology and Visual Sciences to manage daily administrative activities of clinical trials.

You will support the team to reach program goals, assist with recruiting, training, supervising staff, and monitoring the program budget. Responsibilities include coordinating research protocols, maintaining databases, reporting progress to investigators, ensuring IRB compliance, and developing program

Qualifikationen

• Knowledge of biology, chemistry, mathematics, documentation, and records management.
• Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
• Minimum required education and experience stated in job posting.

Aufgaben

• Recruit, screen, enroll and obtain consent from program participants.
• Coordinate research protocols with appointments and procedures, and liaise with other departments.
• Collect, analyze, and disseminate research data and manage databases and files.
• Ensure IRB compliance and prepare regulatory documents and reports.
• Develop program materials, timelines, outreach, and manage study budgets.

Kenntnisse

Biology

Chemistry

Mathematics

Documentation

Records management

Ausbildung

Bachelor’s degree

Jobbeschreibung

The Medical College of Wisconsin, Inc. seeks a Clinical Research Coordinator II in the Department of Ophthalmology and Visual Sciences to manage daily administrative activities of clinical trials.

You will support the team to reach program goals, assist with recruiting, training, supervising staff, and monitoring the program budget. Responsibilities include coordinating research protocols, maintaining databases, reporting progress to investigators, ensuring IRB compliance, and developing program