Clinical Laboratory Director

Abbott

Madison (WI)

On-site

USD 149,000 - 299,000

Full time

14 days+

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Benefits offered by this job

HIP PPO medical plan

High employer retirement contribution

Tuition reimbursement

Free U education benefit

Job summary

Abbott in Madison, WI is seeking a Clinical Laboratory Director to lead development, validation, and ongoing monitoring of diagnostic tests within the Cancer Diagnostics division. You will integrate medical guidelines and CLIA standards to provide guidance and drive test improvements across R&D, Product Development, Medical Affairs, Operations and Quality.

The role requires licensure, board certification in pathology disciplines, and US work authorization, with travel up to 10% to support

Qualifications

Hold a CLIA high-complexity license for a laboratory.
Board certification in related pathology fields as listed.
Authorized to work in the United States without sponsorship.

Responsibilities

Ensure tests meet current medical and technical standards.
Collaborate with commercial, R&D, and operations for test performance.
Monitor test performance, identify trends, and drive improvements.
Support risk assessments and timely resolution of testing concerns.
Stay abreast of guidelines and regulatory standards for tests.

Skills

CLIA license holder

Strong communication

Risk assessment

Team collaboration

Education

American Board of Pathology or ABPath Molecular Pathology certification

ABMGG Laboratory Genetics and Genomics certification

NYS DoH Certificate of Qualification (eligible)

Tools

Bioinformatics

Laboratory Information Systems (LIS)

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Working atAbbott
AtAbbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

Career development with an international company where you can grow the career you dream of.
Employees can qualify for freemedical coveragein ourHealth Investment Plan (HIP) PPOmedical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution.
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
This position works out of our Madison, WI location in the Cancer Diagnostics, legacy Exact Sciences, division. We’re advancing the fight against cancer by delivering innovative diagnostic solutions that help detect, characterize, and monitor disease with greater precision. Our portfolio of molecular and genomic technologies empowers clinicians with actionable insights to support personalized treatment decisions and improve patient outcomes across the cancer care continuum.

As the Clinical Laboratory Director, you be an engaged, key partner working collaboratively across the organization to inform the development, validation, ongoing monitoring, and improvement of our clinical tests. This individual will hold the CLIA license, and will integrate technical expertise, medical guidelines and clinical laboratory standards to deliver clear guidance, drive resolution, and ensure best-in-class test offerings. This dynamic role interacts with Research and Development, Product Development, Medical Affairs, Operations and Quality.

Essential Duties
All responsibilities defined for a CLIA license holder (see CLIA, CAP), with emphasis on representing current technical and medical standards to:

Ensure the technical and medical performance of our tests meet current medical and technical standards (professional societies, regulatory checklists, additional guidelines and standards)
Collaborate with commercial, research and development and operations to ensure test performance, validations
Ensure strong engagement with quality monitoring, quality improvement framework:
Monitor performance of tests, identify trends, evaluate risk, and drive resolution and improvement of test performance
Support escalations, risk assessments and timely resolution of testing concerns
Represent medical and technical standards for best practice
Support clinical consultation
Stay abreast of and integrate emerging guidelines, medical and regulatory standards and apply to current and future test offerings
Coordinate across multiple groups to drive informed, risk-based solutions
Ability to effectively delegate in a matrixed environment
Additional requirements:
Excellent critical thinking, risk assessment and mitigation skills
Strong understanding of technical components of testing, including bioinformatics and Information Technology
Highly collaborative, problem-solving approach
Ability to manage confidential information.
Excellent written and verbal communication skills to convey difficult information in a clear, kind, and respectful manner.
Ability to work in and contribute to a fast-paced, highly collaborative environment.
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
Support and comply with the company’s Quality Management System policies and procedures.
Maintain regular and reliable attendance.
Standing or sitting for long periods of time may be necessary.
Use of computer and some time may be spent concentrating, reading, or analyzing data, or applying scientific rules.
Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for up to approximately 95% of a typical working day.
Ability and means to travel between Exact Sciences locations.
Ability to travel approximately 10% of working time away from work location, may include overnight/weekend travel

Minimum Qualifications

Qualified to hold a CLIA license for a high complexity laboratory:
American Board of Pathology or American Osteopathic Board of Pathology board certification in: Anatomic Pathology or Anatomic and Clinical Pathology Molecular Pathology, or ABMGG Board certification in Laboratory Genetics and Genomics or Molecular Genetics
NYS DoH Certificate of Qualification (or eligible) in relevant discipline(s)
Demonstrated ability to perform the essential duties of the position with or without accommodation.
Authorization to work in the United States without sponsorship.

The base pay for this position is

$149,300.00 – $298,700.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Clinical Affairs / Statistics

DIVISION:

ONCO Cancer Diagnostics

LOCATION:

United States > Madison : 5505 Endeavor Ln

WORK SHIFT:

Standard

TRAVEL: