Clinical Research Coordinator Ii
- Sub-Investigator and coordinator for multiple large, national oncology clinical research studies with enrollments ranging 300-5000 participants per study. - Manages Clinical Trials Assistants team involved in patient screening, enrollment, and data abstraction.- Collaborates with study sponsors and partners to develop and implement protocols, procedures, and regulatory documents. - Prepares and maintains all IRB and regulatory paperwork for select clinical research performed by the PI.- Organizes, Collects, Processes, and Maintains human tissue specimens.- Collaborates with IMR Administration to facilitate contracts for select clinical research performed by the PI.