Clinical Research Coordinator (Oncology)

Clinical Research Coordinator in the Oncology Clinical Trial Support Unit (O-CTSU) specializing in data management and regulatory coordination work. Contributes to the development of processes and tools to support the non-GCP and GCP-related activities associated with study execution. Performs study procedures with accuracy. Conducts all startup, active implementation, and closeout activities. Independently coordinates teams' most complex trials with little to no oversight. Creates corrective and preventative action plans. Develops processes, tools, and training to capture data in accordance with ALCOA-C principles. Manages databases. Monitors site compliance with subject safety reporting, escalates issues, and contributes to the development of tools and processes to enhance subject safety. Contributes to process and tool development to enhance site compliance. Acts as a liaison between investigators, research teams, sponsors, other universities, cooperative groups, other internal and external departments. Runs study meetings. Reviews study forms, databases, and all study-related work for completion and accuracy. Develops standard operating procedures, work-aids and other guidance. Provides mentorship to clinical research staff. Up to 80% remote work permitted.