Clinical Trial Manager overseeing global Phase 3 program for cardiovascular drug development. Responsible for regional study and vendor management while collaborating with clinical operations teams.
About the role
- Clinical Research Nurse coordinating complex clinical trials for RadOnc CRU at University of Pennsylvania. Responsible for patient care and collaboration with research team on clinical activities.
Responsibilities
- Report directly to the Director of RadOnc CRU
- Coordinate complex clinical trials, including subject consent, screening, enrollment, treatment management, & follow-up
- Manage all aspects of clinical studies and all Phases of clinical trials
- Participate in audits by study sponsors, CROs, and the FDA
- Administer medications and contribute to protocol development & SOPs
- Care for study participants in all age groups
- Establish nursing plan of care in collaboration with PI and study team
- Collect, review, and report study data within specified timelines
Requirements
- Bachelor's degree in nursing
- 2-3 years of experience as a Registered Nurse
- Licensure in Commonwealth of Pennsylvania without restriction or limitation
- BSN preferred
Benefits
- Health insurance
- Life insurance
- Flexible Spending Accounts
- Tuition assistance for employee and dependents
- Generous retirement plans including Basic, Matching, and Supplemental options
- Substantial paid time off
- Long-Term Care Insurance
- Wellness and Work-life resources
- Professional and Personal Development resources
- Access to University resources
- Discounts and special services for faculty and staff
- Flexible work hours
- Home Ownership Services
- Adoption Assistance
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