Ophthalmology Clinical Research Coordinator II — Eye Trials

The Medical College of Wisconsin, Inc.; United States; Vor Ort; USD 55.000 - 75.000; Vollzeit

Benefits dieser Stelle

Health insurance

Vision plan

Dental plan

403B retirement package

Tuition reimbursement

Paid parental leave

EFAP

Pet insurance

Onsite fitness facility

Discounts

Zusammenfassung

The Medical College of Wisconsin, Inc. seeks a Clinical Research Coordinator II in the Department of Ophthalmology and Visual Sciences to manage day-to-day clinical research activities, recruit and consent participants, and support staff while helping manage the program budget.

You will coordinate research protocols, train staff, maintain databases, ensure IRB compliance, and report progress to investigators, collaborating across departments and external partners as needed.

Qualifikationen

• Knowledge of biology and chemistry, data analysis, and documentation practices.
• Strong writing and critical thinking skills are essential.
• Experience with research data handling and records management preferred.

Aufgaben

• Recruit, screen, enroll and obtain consent from program participants.
• Coordinate training for program participants.
• Coordinate research protocols with other departments and institutions, maintaining contact with study participants.
• Collect, analyze, and disseminate research data.
• Report program data and progress to study investigators.
• Develop, implement, and maintain comprehensive databases/files related to the program.
• Ensure IRB and regulatory compliance; prepare IRB documents/reports.
• Collaborate on development of program materials and reports.
• Maintain program timeline and coordinate outreach activities.

Kenntnisse

Knowledge of biology and chemistry

Data analysis and problem solving

Documentation and records management

Strong writing skills

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 day-to-day clinical research activities, recruit and consent participants, and support staff while helping manage the program budget.

You will coordinate research protocols, train staff, maintain databases, ensure IRB compliance, and report progress to investigators, collaborating across departments and external partners as needed.