• Stay up-to-date on IQR, OQR, IPFQR, MassHealth CQI, and other regulatory programs assigned. • Support the ITS Regulatory Team's inpatient quality initiatives across the assigned programs to ensure EHR build aligns with associated clinical quality workflows. • Provide regulatory subject matter expertise and act as an internal consultant on assigned work. • Manage large multi-disciplinary regulatory projects. • Analyze workflows and understand policies, procedures, and constraints of the clinical or business operations related to regulatory requirements. • Conduct in-depth and precise investigations and documentation of operational & report specifications. • Analyze new application releases to determine regulatory build and reporting needs. • As requested, evaluate new applications and make recommendations to management. • Act as a mentor to new and less experienced application analysts. • Track, read and analyze new rulemaking and annual updates to existing regulations. • Maintain Epic certifications. • Performs other duties as assigned or as necessary.