Quality and Reg Program Assistant | SQM On-Site
Job in
Moscow, Latah County, Idaho, 83843, USA
Listed on 2026-07-18
Listing for:
Gritman Medical Center
Full Time
position Listed on 2026-07-18
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Job Description & How to Apply Below
Quality and Reg Program Assistant | SQM | Full Time (On-Site)
Job Category: Office, Clerical & Administration
Requisition Number: QUALI
004027
- Posted:
July 13, 2026 - Full-Time
GMC, Gritman Medical Center, 700 S Main St., Moscow, , USA
- Maintain and manage the enterprise-wide quality and regulatory project tracker, including timelines, milestones, deliverables, and responsible parties.
- Track progress of quality improvement initiatives, regulatory action plans, and Joint Commission readiness activities.
- Coordinate follow‑up on assigned tasks from quality committees, regulatory surveys, and executive leadership meetings.
- Identify delays, barriers, and risks in project execution and elevate issues to the Senior Director of Quality & Regulatory Affairs.
- Support implementation tracking for corrective action plans related to audits, surveys, and performance improvement initiatives.
- Maintain documentation systems related to Joint Commission readiness, CMS compliance, and other regulatory requirements.
- Organize and support documentation for accreditation surveys, mock surveys, tracer activities, and compliance audits.
- Assist in preparing materials for regulatory reviews, board reports, and executive presentations.
- Optimize timely collection and organization of evidence required for accreditation and regulatory compliance.
- Coordinate scheduling, agendas, materials, and minutes for quality, patient safety, accreditation, and population health committees.
- Track committee action items and ensure completion of assigned follow‑ups.
- Maintain standardized documentation for committee structures, reporting workflows, and governance requirements.
- Support preparation of executive dashboards, reports, and presentation materials.
- Assist in maintaining quality dashboards, spreadsheets, and tracking tools used for performance monitoring.
- Assist in maintaining the incident event reporting system and associated reports.
- Compile data from multiple departments to support reporting requirements for regulatory and quality programs.
- Support documentation standardization and administrative workflows across quality and regulatory functions.
- Ensure accuracy, consistency, and version control of quality and regulatory documents.
- Serve as a communication hub between clinical quality staff, regulatory teams, ambulatory and hospital leadership, and administrative departments.
- Distribute updates related to quality initiatives, regulatory requirements, and accreditation readiness activities.
- Facilitate timely communication of deadlines, deliverables, and regulatory requirements across departments.
Associates or Bachelors Degree in Healthcare Administration, Business Administration, Public Health, or related field
Required Work experience- 2–5 years of experience in healthcare administration, project coordination, quality support, regulatory compliance, or related field.
- Experience in a hospital, health system, or ambulatory care setting strongly preferred.
- Experience supporting quality improvement, accreditation, or regulatory programs is a plus.
- Strong organizational and project management skills.
- Ability to track multiple projects, deadlines, and priorities simultaneously.
- High attention to detail and accuracy in documentation and reporting.
- Strong communication and interpersonal skills.
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint) and project tracking tools.
- Ability to work effectively with clinical and non‑clinical stakeholders.
- Understanding of healthcare operations, quality programs, or regulatory environments preferred.
- Timely and accurate tracking of quality and regulatory projects.
- Effective coordination of accreditation and regulatory documentation.
- Completion and follow‑up of committee and action items.
- Improved organization and efficiency of quality and regulatory workflows.
- Reduction of administrative burden on clinical quality and leadership teams.
- Support of successful Joint Commission and regulatory survey readiness.
- Provides a positive and professional representation of the organization.
- Promotes a culture of safety…
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