Analyst, Regulatory Programs
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About The Position
The Analyst, Regulatory Programs will serve as a subject matter expert to customers and internal staff by providing expertise to the complexities of their aligning regulatory programs. As a member of our Organizational Development team, your job would involve participating in calls internally and with customers to provide regulatory guidance and expertise, reading and collaborating to interpret and operationalize CMS Proposed and Final Rules, and collaborating with Development and stakeholders to evaluate the impact of product requirements and workflows for successful attestation. You will also participate in Regulatory related cross divisional meetings and collaborations as needed, coordinate and contribute to the development and documentation of the Regulatory Best Practices, and schedule meetings as needed to optimize communication, manage project plans, and follow through with action items. Additionally, you will collaborate to establish and evaluate workflows for accurate report data capture, participate in report testing and creation of patient test data, publish Best Practices to the Regulatory pages, and update the Best Practice Change Log with accurate reflection of edits. Developing internal and external educational resources, facilitating Regulatory Focus Groups, responding to customer and internal questions submitted through the Regulatory Mailbox, assisting with customer regulatory support/issue management, and participating in industry education/forums to build and maintain knowledge of regulatory programs are also key responsibilities. Finally, you will promote and adhere to the Quality Management System guidelines and policies.
