Principal Clinical Molecular Geneticist

Abbott

. Review clinical genetic testing data and test reports .

Posted 9/18/2026full-timeRemote • Illinois • United StatesLead💰 $113,300 - $226,700 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical genetic testing, including data review, report writing, and compliance with laboratory regulations. Proven ability to lead process improvement initiatives and foster effective communication and collaboration within teams.

Highest-signal resume keywords

Doctoral Degree in Chemical, Biological, or Clinical Laboratory ScienceCertification by American Board of Bioanalytics (ABB) as HCLDExperience Performing High Complexity Genetic Testing4+ Years of Experience Reviewing Clinical Test ReportsCurrent New York State Certificate of Qualification

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Genetic TestingData ReviewReport WritingGene Panel CurationTest Methodology SelectionLaboratory ComplianceQuality ManagementProcess ImprovementTechnical TroubleshootingGenetic Variant Interpretation

Soft Skills

CommunicationCollaborationTeamworkConflict ResolutionEmployee Development

Tools & Technologies

Laboratory Information Management SystemsMobile DevicesTabletsComputers

Certifications & Qualifications

American Board of Bioanalytics (ABB) CertificationAmerican Board of Medical Genetics and Genomics (ABMGG) CertificationNew York State Certificate of Qualification

Industry Keywords

Clinical LaboratoryGeneticsSOPsQuality SystemsFederal RegulationsState RegulationsLocal RegulationsHigh-Complexity TestingMolecular GeneticsCytogenetics

About the role

Key responsibilities & impact

Review clinical genetic testing data and test reports
Troubleshoot technical issues and ensure remedial actions are taken
Review scientific literature and interpret genetic variants
Write, edit, and sign out clinical genetic test reports
Curate gene panels using comprehensive literature-supported gene lists
Coordinate and lead process improvement projects focused on cost savings, efficiency, and productivity
Serve as an exception handler and expert resource for complex cases
Participate in test methodology selection and improve systems, processes, and procedures
Develop and coach colleagues
Promote communication, collaboration, employee development, teamwork, and conflict resolution
Communicate with employees, customers, healthcare providers, and vendors, including representing Abbott at conferences
Maintain laboratory compliance with SOPs, quality systems, and professional, federal, state, and local regulations
Uphold Abbott’s mission and values and maintain regular, reliable attendance

Requirements

What you’ll need

Doctoral Degree in a Chemical, Biological, or Clinical Laboratory science from an accredited institution, with required certification
Certification by the American Board of Bioanalytics (ABB) as a High-Complexity Clinical Laboratory Director (HCLD), or by the American Board of Medical Genetics and Genomics (ABMGG) in Laboratory Genetics and Genomics (LGG), Molecular Genetics, or Cytogenetics, or by the Canadian College of Medical Geneticists (CCMG)
Alternatively, Medical Doctor or Doctor of Osteopathic Medicine Degree with 3+ years in a clinical lab with director oversight, certified in anatomical or clinical pathology, or both, by the American Board of Pathology or the American Osteopathic Board of Pathology
Experience performing high complexity genetic testing
4+ years of post-certification experience reviewing and signing out clinical test reports, or 7+ years of total experience reviewing and signing out clinical test reports or equivalent
Current New York state Certificate of Qualification in appropriate areas of oversight as necessary, or ability to obtain within 6 months
Demonstrated ability to perform the essential duties with or without accommodation
Authorization to work in the United States without sponsorship
Ability to manage confidential information
Ability to communicate cross-functionally and establish effective working relationships
Ability to work designated schedules, including nights and/or weekends as needed
Ability to work on a mobile device, tablet, or computer and type for approximately 90% of a typical working day
Ability to travel up to 10% of working time
Compliance with company SOPs, quality management policies, and applicable regulations

Benefits

Comp & perks

Career development with an international company
Excellent retirement savings plan with a high employer contribution
Recognition as a great place to work in dozens of countries worldwide
Recognition as one of the best big companies to work for and best places to work for diversity, working mothers, female executives, and scientists