Lab Compliance & CQI Coordinator
Indexed description
Job Duties And Responsibilities
CLIA Compliance & Laboratory Oversight
- Serve as the primary CLIA compliance resource across all three sites; maintain the organization's posted Certificates of Waiver and associated documentation.
- Serve as primary VFC/VFA Coordinator for all sites.
- Ensure all point-of-care testing (POCT) is performed in accordance with CLIA waiver requirements and manufacturer instructions.
- Maintain quality control (QC) documentation, equipment logs, reagent logs, and temperature monitoring records for all sites.
- Coordinate and track annual lab proficiency testing; ensure timely completion and documentation.
- Conduct periodic internal audits of lab practices at each site; identify deficiencies and develop corrective action plans in coordination with the RN Quality Manager.
- Serve as the primary MA point of contact for external CLIA surveys, HRSA site visits, FTCA reviews, and other compliance audits affecting laboratory services.
- As the subject matter expert, ensures all MA staff in coordination with the MA Training Specialist, maintain CLIA-compliant POCT procedures and documentation requirements, HRSA site visits, FTCA reviews, and other compliance audits affecting laboratory services.
- Monitor for changes in CLIA regulations, CMS guidance, and POCT manufacturer updates; update SOPs accordingly in a timely fashion.
- Partner with the RN Quality Manager to support UDS (Uniform Data System) reporting, HEDIS measure tracking, and clinical quality metric collection.
- Assist in data collection, analysis, and preparation for the organization's annual quality improvement plan.
- Assist with gap analysis on clinical quality metrics at the site and patient panel level; maintain ability to present findings to the Quality team when appropriate.
- Support root cause analysis (RCA) for lab-related incidents, near misses, and quality events; document findings and corrective actions.
- Participate in the organization's Quality Committee; present compliance and CQI updates as requested.
- Assist in implementing evidence-based quality improvement interventions related to preventive care, chronic disease management, and clinical support workflows.
- Own and maintain all laboratory-related policies and standard operating procedures (SOPs) across sites; ensure annual review and updates.
- Maintain organized, audit-ready documentation for all CLIA and compliance-related records.
- Ensure all three sites have consistent, up-to-date reference materials for POCT and lab workflows.
- Community clinic or medical office operations.
- Pertinent federal, state and local laws and regulations regarding issues affecting licensed community clinics, e.g., OSHA requirements.
- Oral and written communication; bilingual (English/Spanish) preferred.
- Organization of work and attention to detail.
- Using standard medical office equipment and performing standard clinic medical and laboratory tests.
- Using a computer for word processing, data entry and e-mail.
- Share the EDCCHC mission and work well in a team environment.
- Develop rapport and work with people of all ages, cultural, religious, social and ethnic backgrounds.
- Be courteous and utilize professional behavior in all interactions with the public and staff.
- Maintain a high level of confidentiality of client information.
- Appropriately deal with difficult situations
- Make decisions within certain prescribed limits according to Policies and Procedures.
- Determine priorities in workload and meet established deadlines.
- Work in a fast-paced environment with frequent interruptions and maintain a positive disposition at all times.
- Be flexible in accepting, changing or carrying out assignments.
- Working knowledge of CLIA regulations, point-of-care testing requirements, and QC documentation standards.
- Experience with UDS reporting, HEDIS measures, or HRSA compliance preferred (FQHC context strongly preferred).
- Strong attention to detail and comfort managing documentation-heavy compliance programs.
- Data literacy: ability to work with spreadsheets, EMR-based quality reports, and basic data analysis.
- Strong written communication skills; ability to draft and maintain clear SOPs and compliance documentation.
- Understands and applies CLIA and HRSA requirements accurately and proactively
- Detail Orientation: Catches documentation gaps before auditors do; maintains airtight records
- Comfortable pulling, interpreting, and presenting clinical quality metrics
- Identifies compliance risks and improvement opportunities without being directed
- Maintains consistency across all sites with different staff and cultures
Education And Certification
- Associate's degree in health sciences, biology, medical assisting, or related field required; Bachelor's preferred.
- Minimum 2–3 years of experience in a clinical setting with direct involvement in lab operations, CLIA compliance, or quality improvement required.
- MA certification (CMA, RMA, CCMA, or equivalent) preferred; phlebotomy certification a plus.
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