Principal Clinical Molecular Geneticist

Abbott•Chicago, IL

8d•$113,300 - $226,700•Remote

About The Position

As a member of the PreventionGenetics team, the Principal Clinical Molecular Geneticist helps lead and advance clinical molecular genetics services within Abbott’s broader cancer diagnostics organization. The role reviews clinical DNA test data and reports, maintains a portfolio of clinical DNA sequencing tests, and cultivates expertise in a subspecialty of genetic disease. It serves as a thought leader among the geneticist team, guides process improvements, and consults on challenging cases. The position requires interpreting genetic variants, curating gene panels, signing out laboratory test results, troubleshooting technical problems, and supporting quality and regulatory compliance. It also provides leadership through coaching, employee development, cross-functional collaboration, communication, and conflict resolution. The position is remote in the United States, with an ability to work nights and/or weekends as needed, a designated schedule, and travel of up to 10% stated in the duties. The job listing separately states “TRAVEL: No.”

Requirements

Doctoral degree in a chemical, biological, or clinical laboratory science from an accredited institution, with qualifying certification maintained throughout employment: ABB High-Complexity Clinical Laboratory Director (HCLD), ABMGG Laboratory Genetics and Genomics (LGG), Molecular Genetics, or Cytogenetics, or CCMG; alternatively, an MD or DO degree with at least 3 years in a clinical laboratory with director oversight and certification in anatomical pathology, clinical pathology, or both by the American Board of Pathology or American Osteopathic Board of Pathology, maintained throughout employment.
Experience performing high-complexity genetic testing.
At least 4 years of post-certification experience reviewing and signing out clinical test reports, or at least 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 it 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 and communicate effectively with employees, customers, health care providers, and vendors.
Ability to thrive in a fast-paced, changing environment and project team situations.
Ability to work the designated schedule, including nights and/or weekends as needed.
Ability to use 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.

Responsibilities

Review genetic testing data; troubleshoot when necessary; review scientific literature; interpret genetic variants; write or edit genetic test reports; and sign out laboratory test results.
Curate gene panels with comprehensive gene lists supported by scientific literature.
Coordinate and lead process improvement projects to drive cost savings, efficiency, and productivity.
Troubleshoot technical problems with technical staff and ensure remedial action when test systems deviate from laboratory performance standards.
Serve as an exception handler and expert resource for colleagues on complex cases.
Participate in selecting test methodology and take initiative to improve systems, processes, and procedures to drive quality in daily production.
Develop and coach others.
Promote communication and collaboration, support employee development initiatives, promote cross-functional teamwork, and aid in conflict resolution.
Manage confidential information and communicate effectively across functions and organizational levels.
Establish and maintain effective working relationships using appropriate interpersonal skills.
Communicate frequently and accurately with employees, customers, health care providers, and vendors, including representing the company at conferences.
Comply with company SOPs, practices, and applicable professional, federal, state, and local regulations, and ensure laboratory compliance.
Support and comply with the company Quality Management System policies and procedures.
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork; model an inclusion mindset.
Maintain regular and reliable attendance and work the designated schedule.
Work nights and/or weekends as needed.
Work on a mobile device, tablet, or computer and perform typing for approximately 90% of a typical working day.
Travel up to 10% of working time, potentially including overnight or weekend travel.