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.
UM
Hybrid Clinical Research Nurse Supervisor
Posted 11 hours ago
About the role
- Clinical Research Nurse Supervisor leading coordination of clinical studies at the Perelman School of Medicine. Overseeing study conduct, compliance, and supervising clinical staff in a hybrid role.
Responsibilities
- Provide leadership in the coordination of IIT and federal or industry sponsored clinical studies/trials
- Oversee study/trial start-up, conduct, and close-out
- Ensure study/trial data integrity and regulatory compliance with GCP guidelines, Federal/FDA regulations
- Supervise CRCs and CRNs as assigned
- Assist with protocol development
- Prepare study SOP, documents, subject binders, tracking logs for study start up
- Provide training and oversight to network sites
- Prepare for and participate in monitoring or audit visits
Requirements
- BSN degree and 5+ years or MSN with 3+ years of experience as a Registered Nurse
- Licensure in the Commonwealth of Pennsylvania without restriction or limitation
Benefits
- Comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
- Flexible spending accounts
- Tuition assistance for employees, spouses, and dependent children
- Generous retirement plans
- Substantial time away from work during the year
- Long-term care insurance
- Wellness and work-life resources
- Professional and personal development resources
- Access to a wide range of University resources and cultural activities
- Discounts and special services for faculty and staff
- Flexible work options including non-traditional hours or job structures
- Forgivable loan for home buying assistance
- Adoption assistance reimbursement
Job title
Job type
Experience level
Salary
Degree requirement
Tech skills
Location requirements
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.
Clinical Research Coordinator managing complex clinical trials in the Neurosurgery department at University of Pennsylvania. Ensures compliance and promotes good clinical practice in research protocols with mentorship responsibilities.
Clinical Research Coordinator overseeing data collection and research tasks at University of Arkansas for Medical Sciences. Analyzing data and training staff in adherence to protocols and quality standards.
Senior Manager, Clinical Scientist at IQVIA leading clinical activities and collaborating with stakeholders. Manage timelines, draft documents, and ensure high - quality deliverables for clinical research.
Associate Director supporting clinical development at Amgen for late - phase oncology trials. Focus on data quality, protocol development, and cross - functional coordination in healthcare innovation.
Lead a team of Clinical Scientists and Medical Writers in Oncology Early Clinical Development at Roche. Focus on innovative trials and regulatory excellence in drug development.
Clinical Research Nurse enhancing pediatric oncology care at Monash Children's Hospital. Collaborating with medical staff and managing patient flow for effective cancer treatment.
Senior Clinical Trial Manager overseeing site management and monitoring for biopharmaceutical solutions organization. Responsible for clinical monitoring, patient safety, and regulatory compliance in South Africa.
Associate HR Partner supporting employee operations at CPS Clinical Research Units. Providing HR guidance and managing employee relations in a clinical environment with on - site presence.