Clinical Research Coordinator

Responsibilities

• Assist with day-to-day study operations, including scheduling, protocol adherence, and coordination of assessments.
• Support participant recruitment, screening, consent procedures, and ongoing communication to ensure retention.
• Collect and manage clinical and research data, including gait, balance, cardiovascular measures, and activity monitoring.
• Assist with treadmill training sessions, monitoring exercise intensity, and documenting training parameters.
• Maintain IRB documentation and ensure strict adherence to study protocols and regulatory compliance.
• Collaborate with investigators and clinical partners across multiple sites.

Requirements

• Bachelor’s Degree.

Preferred Qualifications

• Experience with human subjects or clinical research, including participant interaction and data collection.
• Strong organizational skills and high attention to detail.
• Experience with data entry and management systems such as REDCap.
• Ability to work effectively with clinical populations, specifically individuals with neurological or mobility impairments.
• Familiarity with research protocols and regulatory standards (e.g., IRB, HIPAA).
• Background in exercise science, biomechanics, or rehabilitation.

Benefits

• Medical, dental, and vision insurance.
• 403(b) retirement plan with up to 8% university match.
• Generous time off package.
• Tuition benefits for employees, spouses, and dependents with no payback requirement.

About the Company

Marquette University is a Catholic, Jesuit institution dedicated to the search for truth, the discovery and sharing of knowledge, and the development of leadership expressed in service to others. This position is based in the Integrative Neural Engineering and Rehabilitation Laboratory (INERL) within the Department of Biomedical Engineering, supporting NIH-funded research.