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Are you passionate about healthcare compliance and ready to make a real impact? VOANS Healthcare is seeking a Healthcare Regulatory Specialist to serve as the division’s go-to expert for all regulatory requirements in PACE and Senior Living programs.
Schedule: Monday-Friday 8:00 AM-5:00 PM
Location: Fully Remote
Salary: $90,000-$100,000 (Based on Experience)
About the Job:
The Healthcare Regulatory Specialist is the division’s primary subject matter expert for all regulatory requirements applicable to their assigned business line (PACE or Senior Living). This includes federal regulations, state rules, CMS guidance, contractual obligations (e.g., PACE three-way agreements), and other compliance mandates. The Regulatory Specialist ensures VOANS Healthcare maintains an accurate, current, and operational understanding of these requirements across regions and programs.
Benefit Highlights:
Essentials:
Regulatory Expertise, Interpretation & Consultation
•Serve as the subject matter expert for federal and state regulations applicable to the assigned business line, including CMS requirements, state licensing rules, and contractual obligations (e.g., PACE three-way agreement).
•Provide real-time regulatory consultation to Quality Managers, Clinical Specialists, and program/facility leadership.
•Maintain a centralized repository of regulatory interpretations, guidance documents, and standardized decision tools.
Regulatory Surveillance & Change Management
•Monitor regulatory developments (e.g., CMS memos, state rule changes, federal guidance, association updates).
•Produce concise, actionable regulatory summaries for internal distribution.
•Conduct impact assessments of regulatory changes and outline required operational, documentation, or workflow adjustments.
•Lead planning for compliance with new or revised regulatory requirements, including timelines, responsibilities, and reference materials.
Policy Development & Regulatory Review
•Serve as a primary reviewer of policies and procedures to ensure regulatory accuracy, alignment with federal/state requirements, and internal consistency.
•Maintain policy crosswalks linking regulatory citations to internal policies.
•Participate in drafting and revising policies based on regulatory changes, survey trends, and audit findings.
•Support harmonization of regulatory policy across business lines where appropriate.
Survey Readiness Through Focused Regulatory Audits
•Oversee regulatory components of the internal audit workplan and ensure alignment with survey expectations.
•Conduct focused regulatory audits based on federal/state requirements, areas of known risk, or prior deficiencies.
•Provide documented findings and regulatory interpretations to the Quality Manager and relevant operational leaders.
•Assist Quality Managers and leadership in understanding the regulatory significance of identified issues.
•Maintain readiness tools, crosswalks, and regulatory expectations to support facilities/programs in anticipating survey focus areas.
Internal Audit Program Leadership
•Supervise internal auditors and guide their audit work to ensure accuracy, consistency, and regulatory alignment.
•Ensure audit tools remain up to date with current regulatory requirements and reflect best practices.
•Conduct occasional validation audits (spot checks) to ensure audit integrity and consistency across auditors
•Trend audit findings and prepare reports summarizing regulatory risk patterns, recurring concerns, and opportunities for systemic improvement.
•Collaborate with the VP of Compliance and Performance Excellence and Director of Healthcare Compliance on annual audit workplan development.
Issue Identification & Regulatory Risk Advisement
•Provide regulatory interpretation of issues identified through:
Internal audits
Incidents
Complaints/grievances
Survey findings
Operational escalation
•Ensure the regulatory implications of issues are clearly communicated to the Quality Manager and leadership.
•Advise on what regulatory standards apply, what outcomes must be achieved, and what the minimum regulatory expectation for resolution looks like.
•Collaborate with QMs during the preliminary review of findings to ensure accurate problem definition prior to corrective action planning.
•Support leadership awareness of high-risk regulatory trends and systemic vulnerabilities.
Education, Training & Regulatory Competency Development
•Provide training on the regulatory topics most relevant to the assigned business line.
•Develop regulatory quick reference guides, checklists, and decision aids for Quality Managers, Clinical Specialists, and operational leaders.
•Support onboarding and ongoing competency development for Quality Managers.
•Deliver targeted education following regulatory changes or identified gaps.
High-Risk Process Oversight (Business-Line Specific)
•Senior Living Specialist:
Serve as regulatory resource for infection control, care planning, accident prevention, abuse/ neglect standards, psychotropic medication regulations, PCC documentation expectations, and MDS compliance (in coordination with MDS Manager).
Support facilities in understanding and implementing survey expectations related to these domains.
•PACE Specialist:
Serve as regulatory resource for participant rights, IDT processes, service authorization timeliness, homecare supervisory expectations, contracted provider compliance, grievances/ appeals, and adherence to the PACE three-way agreement.
Support interpretation of CMS audit protocols and expectations for core PACE domains.
Data, Metrics & Dashboard Collaboration
•Identify regulatory performance indicators suitable for dashboard reporting.
•Partner with BI/PBI resources to integrate regulatory metrics into division-wide dashboards.
•Provide analysis and regulatory interpretation of trends in incidents, audits, survey results, and compliance indicators.
Cross-Business-Line Integration & Collaboration
•Promote consistency in regulatory practice across regions and business lines.
•Participate in cross-functional quality and compliance committees.
•Contribute to initiatives focused on standardizing processes, reducing variation, and improving regulatory reliability.
Regulatory Relationship Management
•Maintain positive working relationships with state regulatory bodies, CMS staff, and provider associations.
•Participate in state or regional regulatory meetings, provider forums, or rulemaking sessions as appropriate.
•Serve as a professional, informed point of contact for regulatory matters.
Other:
Required Qualifications:
At VOANS, we celebrate sharing, encouraging and embracing diversity. Equal employment opportunities are available to all without regard to race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, parental status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. We believe that blending individual strengths and unique personal differences nurtures and supports our organizations’ shared commitment to our mission and creates an inclusive and diverse environment where everyone feels valued and has the opportunity to do their personal best
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