[Hiring] Associate Clinical Analyst II @GeneDx

Role Description

The Associate Clinical Analyst II (ABMGG-eligible or active candidate) supports the interpretation of genetic findings and contributes to accurate diagnosis and case resolution through exome and genome sequencing. This entry-level role focuses on building foundational clinical analysis skills by assisting with case reviews under supervision, performing routine data interpretation tasks.

• Support variant classification activities
• Prepare accurate documentation
• Contribute to internal database updates
• Ensure timely documentation and maintain quality standards
• Aid departmental initiatives through collaborative engagement and continuous learning

Shift: Tuesday-Saturday or Sunday-Thursday 9am-5pm ET

Job Responsibilities

• Perform clinical data analysis and case management to accurately interpret genetic findings
• Establish phenotype-genotype correlations across diverse genetic disorders
• Investigate and interpret clinical features of genetic conditions using internal resources and professional tools
• Review and finalize genetic test reports, interpret variants, and curate internal databases
• Serve as a subject matter expert for designated genes, disorders, tests, and workflows
• Communicate with clients via email, phone, or other channels to support case resolution and provider engagement
• May abstract clinical information from patient records
• Perform literature reviews and database searches to support variant interpretation and classification
• Meet or exceed productivity and error standards as assigned by team lead
• Document evidence and rationale for variant classification in a clear, standardized format
• Assist with development of variant-, gene-, or disease-specific test information and report language
• Perform other duties as assigned to support the team or department

Credential-specific responsibilities include but are not limited to:

• Consultation Availability: Provides timely consultation to ordering providers regarding test selection, interpretation, and clinical correlation of laboratory results
• Report Oversight: Reviews and ensures laboratory reports meet CLIA and CAP requirements for accuracy, completeness, and clinical relevance
• Result Authorization: Approves and signs off on high-complexity test results in accordance with CLIA regulations

Qualifications

• PhD in Biology, Genetics or related field, MD or DO with more than 2 years directly relevant experience in clinical diagnostics (including fellowship)
• Excellent verbal and written communication skills
• Demonstrated computer skills, including ability to maintain high proficiency with internal systems and Microsoft Office Suite and the Office 365 environment
• Prior experience with variant curation is preferred but not required

Certificates, Licenses, Registrations

• ABMGG certification or equivalent, certified in at least one specialty OR board eligible

Physical Demands

• Prolonged periods of sitting or working at a computer in a home office environment
• Occasional need to lift or move materials or equipment weighing up to 20 pounds during travel or team visits

Work Environment

• Frequent use of digital communication platforms (e.g. video conferencing, email, and collaboration tools)
• Ability to focus and manage complex tasks in a remote setting with multiple concurrent priorities
• May require occasional travel to laboratory sites, corporate offices, or conferences (typically <10%)

Pay Transparency, Budgeted Range

$150,000 — $165,000 USD

Benefits

• Paid Time Off (PTO)
• Health, Dental, Vision and Life insurance
• 401k Retirement Savings Plan
• Employee Discounts
• Voluntary benefits

Company Description

At GeneDx, we create, follow, and are informed by cutting-edge science. With over 20 years of expertise in diagnosing rare disorders and diseases, and pioneering work in the identification of new disease-causing genes, our commitment to genetic disease detection, discovery, and diagnosis is based on sound science and is focused on enhancing patient care.

• Experts in what matters most
• High-quality testing: Our laboratory is CLIA certified and CAP accredited and most of our tests are also New York State approved
• Advanced detection: By interrogating genes for complex variants, we can identify the underlying causes of conditions that may otherwise be missed
• Thorough analysis: We classify variants according to our custom adaptation of the most recent guidelines
• Customized care: Our experts review all test results and write reports in a clear, concise, and personalized way
• Impactful discovery: Our researchers continue working to find answers even after testing is complete