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LIS Coordinator

Labcorp


Job Location:

Nashville, IN - USA

Monthly Salary: Not provided by the employer
Posted: 16 September 2026 (16 hours ago)
Application Deadline: 14 December 2026
Vacancies: 1 Vacancy

Job Summary


Labcorp is a global leader in laboratory services providing the insights and answers that help healthcare providers patients researchers pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science data technology and laboratory network we advance diagnostics accelerate innovation and help address some of the worlds most important health challenges. As we shape the future of healthcare we are leveraging advanced technologies intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise youll have the opportunity to do meaningful work grow your career and make a real impact on peoples health around the world. Together were improving health and improving lives.


LabCorpis seeking a LIS Coordinatorto join our teamat Ascension St Thomas West Hospital in Nashville Tennessee.

Work Schedule: 1st shift; Monday - Friday 8:00am - 4:30pm. On call when needed. Hours may be adjusted based on business needs or at the discretion of the hiring manager.

Job Responsibilities:

  • MonitorLISdashboards for basic system alerts error queues and analyzer connectivity flags.

  • Assistwith routine configuration updates such as label formats print routing user role changes and test dictionary documentation.

  • Coordinate workstation printer and peripheral device support with IT/LISAnalysts.

  • Performfirstleveltroubleshooting and escalate issues withappropriate details.

  • Assistswith testing and validation activities

  • Execute predefined test scripts during upgrades patches and workflow changes.

  • Document validation results and communicate findings toLISAnalysts.

  • Support comparison of preandpostchangefunctionality toidentifybasic discrepancies.

  • Helpmaintaintest evidence andvalidationdocumentation libraries.

  • Assistwithuseraccessreviews andLISpermissions auditing.

  • Run routine audit logs (e.g. pendinglists workflow exceptions) per SOP.

  • Reportobservedworkflow or data discrepancies to Analysts or leadership.

  • Support regulatory preparation by gatheringLISaudit outputs as instructed.

  • Maintain downtime binders forms labels instructions and communicationlists.

  • Participate in downtime drills and document observations.

  • Assistwithpostdowntimevalidation steps by following checklists.

  • Help update downtime and DR documentation as workflows evolve.

  • Provide basicLISnavigationassistanceand respond to routine user questions.

  • Coordinate and scheduleLIStraining sessions with Analysts andleadership.

  • Maintain training guides tip sheets and learning materials.

  • Supportonboarding ofnew laboratory staff withLISorientation tasks.

  • Run scheduled operational and quality reports usingLIStools.

  • Performfirstleveldata review and flag anomalies for Analysts or leadership.

  • Distribute recurring reports to appropriate stakeholders.

  • Maintain reporting schedules and documentation.

Minimum Qualifications:

  • Associates degree in a Chemical or Biological science Clinical Laboratory Science Medical TechnologyInformation Technology/Computer Science

  • 1 year ormore ofexperience in a clinical laboratory IT support environment.

Preferred Qualifications:

  • Bachelors degreein a Chemical or Biological science Clinical Laboratory Science Medical TechnologyInformation Technology/Computer Science

  • ASCP and/or AMT Certifications

  • 2 years or more of experience supervising or leading a team

  • Prior experience supporting or administering anLISor EHR systems in a hospital or healthcare setting

  • 2 years of experience with laboratory workflows across multiple disciplines (chemistry hematology microbiology blood bank etc.)

Additional Job Standards:

  • In lieu of education requirementslisted above non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirement

Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical Dental Vision Life STD/LTD 401(k) Paid Time Off (PTO) or Flexible Time Off (FTO) Tuition Reimbursement and Employee Stock Purchase Plan.Employees regularly scheduled to work less than 20hoursCasual Intern and Temporary employees are only eligible toparticipatein the 401(k) Plan.Employees who are regularly scheduled toworka 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information pleaseclick here.


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race religion color national origin sex (including pregnancy childbirth or related medical conditions) family or parental status marital civil union or domestic partnership status sexual orientation gender identity gender expression personal appearance age veteran status disability genetic information or any other legally protected characteristic. Additionally all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.


We encourage all to apply

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Required Experience:

IC


About Company

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Labcorp helps patients, providers, organizations, and biopharma companies to guide vital healthcare decisions each and every day.

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