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.
PC
Onsite Clinical Research Coordinator, Neurosurgery
Posted 1 hour ago
About the role
- 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.
Responsibilities
- Facilitate, promote, and ensure good clinical practice in research protocols
- Independently manage different phases of complex clinical trials
- Mentor coordinators and research assistants
- Work with partnering institutions on management of multisite trials
- Participate in meetings related to protocols, training, and compliance
- Process specimens as required per trial guidelines
- Administer investigational product and study-related medications
Requirements
- Bachelor of Science
- 2 to 3 years of experience or equivalent combination of education and experience
- Must adhere to University guidelines and FDA regulations
- Ability to prepare and process all documentation for clinical trials
- Coordinate and maintain all required documentation
- Schedule patient visits and testing as necessary
- Conduct initiation, monitoring, and closeout visits with sponsors/CROs
- Ensure proper reporting of adverse events and manage treatment administration
Benefits
- Health insurance
- Life insurance
- Flexible Spending Accounts
- Tuition benefits for employees and families
- Retirement plans
- Paid time off
- Long-Term Care Insurance
- Wellness and Work-life Resources
- Professional and Personal Development resources
- University resources and access
- Discounts and Special Services
- Flexible work hours
- Home Ownership Services
- Adoption Assistance
Job title
Job type
Experience level
Salary
Degree requirement
Location requirements
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.
Clinical Research Study Assistant involved in Alzheimer's disease research collecting samples and data. Participating in study protocols and maintaining participant interactions.
Oncology Clinical Research Coordinator at WVU managing clinical trials and ensuring protocol compliance. Collaborating with research staff and healthcare providers while advocating for ethical participant care.