Associate Director/Director, Molecular Diagnostics

New York Genome Center•New York, NY

15h•$177,000 - $250,000•Onsite

About The Position

The Associate Director/Director will be responsible for analysis, interpretation, and reporting of molecular diagnostic tests and screening results such as genome sequencing for Constitutional Genomics, carrier screening, or Oncology assays including MRD. This individual will contribute significantly to new clinical research and assay development and to improving the existing infrastructure of variant filtering and prioritization for clinical reporting. This is an exciting opportunity for the right candidate to join a state-of-art clinical genomics laboratory and an expanding world-class next-generation genome center.

Requirements

PhD or MD in biology, genetics, biochemistry, or a related field.
ABMGG Board certified in Clinical Molecular Genetics and Genomics, or Laboratory Genetics and Genomics, or Board certified in Molecular Genomic Pathology.
New York State Certificate of Qualification in genetic testing or Oncology Molecular and Cellular Tumor Markers required.
ABMGG Board certified required.
Thrives in a fast-paced, rapidly changing, start-up like environment.
Experience with genetic variant classification as per ACMG/GlinGen guidelines and/or somatic variant classification as per AMP guidelines; Knowledge of phenotype ontologies.
Self-motivated and capable of analyzing and solving complex problems through innovative thought and experience.
Excellent verbal and written communication skills and organizational skills are essential for this role.

Nice To Haves

At least 4 years of post-board-certification experience in the interpretation and reporting of Exome or Genome Sequencing data and/or large-scale carrier screening is preferred for candidates at the Associate Director level, and at least 6 years of post-board-certification experience in these areas is preferred for candidates at the Director level
Prior experience working in a high-volume molecular diagnostic/clinical laboratory.
Proven track record of hands-on experience in Exome/Genome Sequencing.
Experience establishing, validating, and/or analyzing large-scale carrier screening programs is preferred.
Experience with oncology molecular testing, including minimal residual disease (MRD) testing, is preferred.

Responsibilities

Identify, annotate and investigate the clinical significance of genetic variants found in NGS-based molecular assays for undiagnosed genetic diseases, or carrier screening, or tumor sequencing.
Interpret and sign out reports for clinical genome sequencing from various research and clinical projects.
Work closely with the Senior Director/lab leadership to develop and validate new NGS based tests and other translational research projects. Assist in creation of an efficient and scalable infrastructure for a high-volume clinical testing laboratory.
Co-lead efforts to integrate genome sequencing into medical practice.
Mentor junior team members.
Responsible for creation and dissemination of precision medicine knowledge of variant-disease associations in the context of genetic disorders.
Responsible for improving the existing infrastructure of variant filtering and prioritization used for clinical reporting.
Participate in educational activities in the Clinical Laboratory.
Communicate effectively and be able to explain the test results to the ordering provider and recommend additional testing.