Temporary CLIA Laboratory Quality Manager

University of North Texas System

$75K — $95K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in healthcare administration, business, law, or related field; Master's preferred.
  • Ten years of experience in healthcare, hospital, and/or academic medicine, or equivalent combination of education, experience, and training.
  • ASCP certification (MT, MLS, or equivalent) and CAP accreditation strongly preferred.
  • 5-8 years of laboratory experience, with at least 2 years in QC/QA or compliance focused role.
  • Direct experience with CLIA regulations and lab certification processes.

Responsibilities

  • Design and implement all Quality Management System (QMS) policies and procedures.
  • Investigate errors or unexpected results, document corrective actions, and communicate QC metrics regularly.
  • Maintain audit-ready records for compliance with CLIA, CAP, HIPAA, and state/local regulations.
  • Lead laboratory through the CLIA certification process from application to approval.
  • Serve as the primary inspection contact for CLIA, CAP, state, and federal regulators.
  • Manage proficiency testing programs and oversee daily lab workflows for efficiency and accuracy.
  • Monitor calibration records, maintenance logs, and QA/QC perspectives across lab operations.

Benefits

  • Eligible for TRS retirement benefits.
Full Job Description
Temporary CLIA Laboratory Quality Manager

Job no: 514526
Work type: Staff
Location: Fort Worth
Categories: Compliance

Title: Temporary CLIA Laboratory Quality Manager

Employee Classification: Senior Compliance Officer

Campus: University of North Texas - Health Science Center

Division: HSC-Div of Rsrch & Innovation

SubDivision-Department: HSC-Health Institutes & Centers

Department: HSC-Inst Translational Research-304700

Job Location: Fort Worth

Salary: Commensurate with experience

FTE: 1.000000

Retirement Eligibility: TRS Eligible

Department Summary

The Institute for Translational Research is devoted to bringing novel diagnostics and interventions to patients and families suffering from neurodegenerative diseases, fostering translational research in neurodegenerative diseases at UNTHSC, and Create solutions for a healthier community. Our team spans basic "bench-top" science, clinical research, community-based research and clinical trials. Our translational approach is intended to foster discovery and expedite those discoveries toward the benefit of those suffering from brain disease. A particular emphasis of ITR is the development of personalized (or person-focused) medicine for Alzheimer's disease.

Position Overview

This temporary role will support laboratory preparation and CLIA certification while overseeing quality control and quality assurance processes, regulatory compliance, operational readiness, and laboratory documentation and reporting. These responsibilities are critical to ensuring compliance with CLIA regulations and institutional standards while supporting the laboratory's successful implementation and ongoing operations.

Minimum Qualifications

Bachelor's degree in healthcare administration, business, law or closely related field, and ten years of experience in healthcare, hospital and/or academic medicine, or any equivalent combination of education, experience and training.

Knowledge, Skills and Abilities

  • Senior Leadership Skills
  • Communication Skills
  • Start up and built from scratch lab environment experience
  • Strong Documentation Skills


Preferred Qualifications

  • Bachelor's degree in Medical Laboratory Science, Biology, Chemistry, or related field
    (Master's preferred)
  • ASCP certification (MT, MLS, or equivalent) and CAP accreditation strongly preferred
  • 5-8 years of laboratory experience, with at least 2 years in a QC/QA or compliance focused role
  • Direct experience with CLIA regulations and lab certification processes


Job Duties

  • Design and implement all QMS policies, procedures, and daily checks.
  • Investigate any errors, failures, or unexpected results and document corrective actions and preventative actions. Flag risks early, ensure every test meets federal and state regulations, proper documentation and response to all internal and external audits and report QC metrics and compliance status to leadership on a regular basis.
  • Maintain QC and QA records that are audit-ready at all times, all regulatory requirements_CLIA, CAP, HIPAA, and applicable local and state regulations, build and maintain the QMS and Standard Operating Procedures (SOP).
  • Lead the lab through the CLIA certification process from application to approval - (Essential)
  • Serve as the primary point of contact for inspections (CLIA, CAP, state, federal) - (Essential)
  • Manage proficiency testing programs and ensure timely submission, oversee daily lab workflows to ensure efficiency and accuracy.
  • Monitor incidents/deviations, calibration records, maintenance logs, and vendor relationships,internal audits and continual quality improvement, environmental conditions, and reagent and supply inventory from a QA/QC perspective and environmental conditions, and reagent and supply inventory from a QA/QC perspective.


Physical Requirements

  • Repeating motions that may include the wrists, hands and/or fingers.
  • Sedentary work that primarily involves sitting/standing.
  • Lifting and Moving objects up to 20 pounds.
  • Communicating with others to exchange information.


Environmental Hazards

  • Sedentary work that primarily involves sitting/standing.


Work Schedule

Monday - Friday 8a-5p On Site

Driving University Vehicle

No

Security Sensitive

This is a Security Sensitive Position.

Special Instructions

Applicants must submit a minimum of two professional references as part of their application. If needed, additional references can be added after the application has been submitted.

Benefits

For information regarding our Benefits, click here.

Advertised: 08 Jul 2026 Central Daylight Time
Applications close:

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