Clinical Research Nurse D

Provides leadership in the coordination of clinical trials and unit-related projects. Oversees study approvals, participant enrollment and consent, visit scheduling, medication administration, data collection, and regulatory documentation to ensure compliance with institutional and sponsor requirements.

Requirements

• Ensure proper screening and enrollment of all study participants
• Ensure proper reporting of serious and non-serious adverse events
• Coordinate the administration of the investigational product and study related medications
• Meet with Principal Investigator routinely to discuss study related issues
• Ensure preparation of all required study related documents for submission
• Manage scheduling and coordination of subject study specified treatment, follow-up visits and procedures
• Manage collection of data from source documents pertaining to study visits and transcribe to case report form

Benefits

• Comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
• Flexible spending accounts to pay for eligible health care and dependent care expenses
• Tuition assistance for employee, spouse, and dependent children
• Generous retirement plans
• Time away from work during the course of the year
• Long-term care insurance
• Wellness and work-life resources
• Professional and personal development resources
• University resources and cultural and recreational activities
• Discounts and special services