Director of Federal and Integrated Regulatory Guidance NY

Position Overview Empower. Unite. Care.

Metro Plus
Health
is committed to empowering New Yorkers by uniting communities through care. We believe that Health care is a right, not a privilege. If you have compassion and a collaborative spirit, work with us. You can come to work being proud of what you do every day.

The Director, Federal and Integrated Regulatory Guidance will oversee regulatory guidance for the Plan’s Medicare Advantage and Integrated Products. This involves daily monitoring of state and federal communications, analyzing guidance and translating into simple language for the respective impacted business areas. The Director will work to develop implementation strategies and specific operational activities to support timely and compliant implementation, while providing ongoing guidance and support throughout the life cycle of implementation projects.

The Director will monitor proposed guidance, share changes and impact with leadership and solicit feedback as a means to contribute to state and federal policy development. The Director also advises the sales and marketing team as to permissible activities for marketing and outreach campaigns and related collateral. The Director will directly supervise a team of two.

• Track state and federal regulatory changes for purposes of disseminating information to business leads in easy to understand terminology, develop implementation approach and basic set of activities required to comply with regulatory change.
• Participate and collaborate with cross functional work groups established to implement regulatory changes.
• Monitor proposed state and federal guidance, solicit input from impacted business leaders.
• Advise sales and marketing team as to permissible activities for marketing and outreach campaigns and related collateral.
• Review and update Policies and Procedures to ensure content is aligned with current regulatory standards.
• Track Medicare local coverage determinations to assist in policy and procedure review and development.
• Inform Senior and Executive Staff of potential compliance issues, delays in implementing regulatory and/or policy changes.
• Provide feedback to direct reports on a regular basis as to performance, progress with meeting team goals.
• Engage with direct reports to identify team members’ goals for career path, areas for improvement.
• Other duties as assigned or requested.

• Bachelor’s degree required
• 5 years’ experience with Medicare and Integrated (Duals) products
• 5 years’ experience in a compliance, regulatory affairs, or government affairs function within a Managed Care Organization.
• Knowledge of CMS rules and regulations as it relates to Medicare products and integrated/dual eligible plans
• Understanding of managed care operations
• Experience managing complicated projects, keeping track of details, and staging work to deliver projects on time
• Proven ability to articulate regulatory requirements to business and technical staff to capture information and achieve results

• None

• Solid Microsoft Excel skills and strong proficiency using MS Word, Excel and PowerPoint and SharePoint.
• High-level of skill in leading interdepartmental and cross-functional strategy development; experience managing professional staff on multiple projects to ensure corporate deadlines and objectives are met. Simultaneously, manage multiple projects.
• Excellent oral, written, analytical and presentation skills required.
• Ability to interpret regulatory guidance and summarize guidance.
• Ability to multi-task various projects at the same time.
• The utmost integrity in the discreet and confidential handling of confidential materials is necessary.

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