The opportunity
Associate/Laboratory Director of Oncology, Comprehensive Genomic Profiling
What you'll do
Provide clinical sign-out and interpretation for CGP reports, identifying: actionable biomarkers and relevant clinical trials
Provide technical and clinical support for laboratory staff, genetic counselors, and other clinical personnel
Ensure acceptable levels of analytical performance for CGP assays, compliance: with applicable standards, and laboratory inspection-readiness at all times
Troubleshoot workflow and laboratory issues with clinical care and regulatory standards in mind
Document findings and maintain accurate records consistent with Natera policies and procedures
Test reports include pertinent information for test interpretation, and
What they're looking for
- Availability for consultation concerning test results and the interpretation: of those results as they relate to specific patient conditions
- Education: MD/DO and/or PhD in genetics or related field required.
- Board Certification: ABMGG board-certified in Clinical Cytogenetics and/or Molecular Genetics, ABP board-certified in Molecular Genetic Pathology, or equivalent doctoral-level board required.
- Licensure: Current California laboratory director license as a Clinical: Genetic Molecular Biologist or Clinical Cytogeneticist required. Candidates eligible for license may be considered.