Clinical Research Associate, Orthopedics

Description What You Will Do

• Responsibilities include overseeing study and regulatory operations including startup, maintenance and closeout for multiple multi-center, international clinical research studies, protocol compliance, regulatory binders and documentation, imaging manuals/ grading manuals, quality control, and data monitoring and reporting.
• Provides support and database maintenance for ongoing research programs in database reviews and developing reports and tables documenting study status.
• Facilitate query resolution related to both certification and study image submissions.
• Provide support to the Directors, the clinical research project specialist and the Program coordinators.

• Performs other duties as assigned.
• Complies with all policies and standards.
• For specific duties and responsibilities, refer to documentation provided by the department during orientation.
• Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.