About this role

Coordinate and supervise clinical research studies providing operational support
Ensure adherence to study protocols, regulatory requirements, and radiation safety standards
Manage detailed project operations and oversee the study team
Provide cross-functional support to Clinical Research Coordinators

Bachelor's Degree with 3-5 years of related experience or equivalent combination of education and experience
Strong problem-solving, communication, and writing skills
Excellent organizational and time management abilities
Knowledge of IRB and human research protection regulations
Strong attention to detail and ability to multitask

Comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
Flexible spending accounts for eligible health care and dependent care expenses
Exceptional tuition benefits for employees, spouses, and dependent children
Generous retirement plans including Basic, Matching, and Supplemental options
Substantial paid time off for vacations and personal affairs
Long-term care insurance for staff and eligible family members
Various wellness programs and resources
Professional and personal development resources
Access to University resources and cultural activities
Discounts on goods and services

Clinical Research Project Manager

Key skills