• Develop, author, assemble, publish and submit IDE Annual Reports, Post-Approval Study Annual Reports, and PMA Annual Reports. • Work collaboratively with subject matter experts and business partners to identify and gather data required for submission. • Monitor regulatory changes and assess their impact on organizational processes and products. • Review and approve technical documentation to ensure alignment with the PMAs. • Maintain FDA device listing and site registration. • Collaborate with stakeholders such as R&D, Engineering, Quality, Clinical and Operations teams.

• 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.

• Own the compliance agenda end-to-end: readiness for VARA expectations, ongoing supervision, and scalable controls as volumes grow. • Operate as VARA’s day-to-day interface, with the CEO still expected to demonstrate clear judgement and credibility during regulator engagement. • Establish credibility with VARA early; preference for leaders with prior UAE regulatory engagement—an existing relationship materially de-risks the set-up. • Act as connective tissue between Dubai market realities and Coins.ph leadership, keeping the build aligned to international expansion priorities. • Builder mentality: hands-on, comfortable with ambiguity, able to create momentum fast from a standing start. • Commercial + compliance maturity: move fast, but never at the expense of regulatory credibility and control integrity.

• Provide Compliance Program leadership for assigned service lines and/or locations. • Responsible for the assisting in the overall implementation and day-to-day management of the Revenue Cycle compliance program. • Works collaboratively on program components, standards, goals, resources, training, monitoring, reporting and team building efforts. • Work cooperatively with Company Leaders to ensure continuing support and understanding of all compliance responsibilities. • Serve as Compliance liaison to Ensemble clients. • Develop and perform training associated with Compliance Program policies, regulatory updates, government and payer coding audits, investigations, and settlements.