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Clinical Cytogeneticist

Job in Phoenix, Maricopa County, Arizona, 85003, USA
Listing for: Sonora Quest Laboratories
Full Time position
Listed on 2026-08-26
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 195000 - 235000 USD Yearly USD 195000.00 235000.00 YEAR
Job Description & How to Apply Below

Sonora Quest Laboratories seeks a Cytogenetics Clinical Director to lead our high-complexity cytogenetics laboratory within Healthcare & Medical Services. The Director will oversee cytogenetic and FISH testing, provide expert clinical interpretation, and ensure rigorous quality and regulatory compliance. You will guide assay development, mentor a collaborative team, and partner with clinicians across oncology and genetic services. Join a culture that values innovation, professional growth, and diverse perspectives while advancing cutting-edge diagnostic solutions for patients.

Responsibilities

  • Provide clinical and scientific leadership for the cytogenetics laboratory
  • Oversee design, validation, and implementation of cytogenetic and FISH assays
  • Review, interpret, and sign out cytogenetic results and clinical reports
  • Ensure CLIA/CAP and other regulatory compliance and quality assurance
  • Collaborate with pathologists, oncologists, and genetic counselors on complex cases
  • Develop and update laboratory policies, procedures, and testing algorithms
  • Lead, mentor, and evaluate technical and professional staff
  • Drive innovation, workflow optimization, and adoption of new technologies
  • Participate in case conferences, tumor boards, and clinician education
  • Contribute to research, publications, and continuous process improvement

Required Skills

  • Clinical cytogenetics interpretation
  • FISH and karyotyping methodologies
  • Molecular cytogenetics techniques
  • Laboratory quality management (CLIA/CAP standards)
  • Laboratory information systems (LIS) usage
  • Oncology and constitutional genetics knowledge
  • Assay development and validation
  • Regulatory compliance and accreditation preparation
  • Leadership and team management
  • Clinical report writing and documentation
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