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Abbott

Principal Clinical Molecular Geneticist

Abbott

. Review clinical genetic testing data and test reports .

Posted 10/28/2026full-timeRemote • United StatesLead💰 $113,300 - $226,700 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Expertise in reviewing and interpreting clinical genetic testing data, ensuring laboratory compliance with regulations, and leading process improvement initiatives. Strong communication and collaboration skills are essential for effective cross-functional interaction and employee development.

Highest-signal resume keywords
Doctoral Degree In Chemical, Biological, Or Clinical Laboratory ScienceCertification By ABB As HCLD, ABMGG In LGG, Molecular Genetics, Or Cytogenetics4+ Years Experience Reviewing And Signing Out Clinical Test ReportsCurrent New York State Certificate Of QualificationCompliance With Company SOPs And Regulations

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Genetic Testing Data ReviewGenetic Variant InterpretationLaboratory Test Result Sign-OutGene Panel CurationProcess Improvement Project LeadershipTest Methodology SelectionTechnical Problem TroubleshootingQuality Management Compliance
Soft Skills
Effective CommunicationCollaborationEmployee DevelopmentConflict ResolutionAdaptability In Fast-Paced Environments
Tools & Technologies
Mobile DevicesTabletsComputers
Certifications & Qualifications
HCLD CertificationABMGG CertificationCCMG CertificationAmerican Board Of Pathology CertificationAmerican Osteopathic Board Of Pathology Certification
Industry Keywords
Clinical LaboratorySOP ComplianceQuality Management PoliciesFederal RegulationsState Regulations

About the role

Key responsibilities & impact
  • Review clinical genetic testing data and test reports
  • Troubleshoot testing issues and review scientific literature
  • Interpret genetic variants and write/edit genetic test reports
  • Sign out laboratory test results
  • Curate gene panels with comprehensive, literature-supported gene lists
  • Lead process improvement projects focused on cost savings, efficiency, and productivity
  • Troubleshoot technical problems and ensure remedial actions are taken
  • 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 others
  • Promote communication, collaboration, employee development, and conflict resolution
  • Communicate cross-functionally across company levels
  • Represent the company at conferences
  • Ensure laboratory compliance with SOPs, quality management policies, and applicable regulations
  • Uphold Abbott’s mission and values
  • Maintain regular and reliable attendance

Requirements

What you’ll need
  • Doctoral Degree in a Chemical, Biological, or Clinical Laboratory science from an accredited institution, plus certification by ABB as HCLD, ABMGG in LGG, Molecular Genetics, or Cytogenetics, or CCMG
  • 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 American Osteopathic Board of Pathology
  • 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, 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 effectively with employees, customers, health care providers, and vendors
  • Ability to work in a fast-paced, changing environment and project teams
  • Compliance with company SOPs, practices, professional, Federal, State, and local regulations
  • Ability to work designated schedules, including nights and/or weekends as needed
  • Ability to use mobile devices, tablets, and computers and type for approximately 90% of a typical working day
  • Ability to travel up to 10% of working time, including possible overnight/weekend travel

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 and a highly admired company
  • Work environment recognized for diversity, working mothers, female executives, and scientists