Research Study Assistant II - Cancer Clinical and Translation Office - 40 Hours - Days

GENERAL SUMMARY:

Under supervision the Research Associate:

• Coordinates low-moderate complexity clinical research projects in compliance with the Code of Federal Regulations.
• Provides technical support to Principal Investigators.
• Analyzes protocol specific requirements and implements measures to ensure physician, patient, and clinician compliance.
• Reviews medical record and compiles data into sponsor provided database in support of the primary endpoint of the clinical trial.
• Identifies and reports adverse events to medical monitor, FDA, and all other governing bodies.
• Coordinates all external audits and monitoring visits and serves as liaison between institution and sponsor.
• Serves as departmental and system-wide resource.