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GeneDx

Associate Variant Scientist

Posted Yesterday
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Remote
Hiring Remotely in USA
80K-100K Annually
Entry level
Remote
Hiring Remotely in USA
80K-100K Annually
Entry level
Independently review genomic data across multiple platforms to evaluate pathogenicity of sequence and copy-number variants, document findings for reporting, meet productivity and accuracy targets, participate in continuing education, and assist with training and case review as needed to support clinical diagnostics.
The summary above was generated by AI

At GeneDx (Nasdaq: WGS), we don’t just diagnose rare diseases — we redefine what’s possible in precision medicine. With one of the world’s largest, rare disease datasets, we turn genomic data into answers that change lives and accelerate discovery. Patients and families around the world are counting on us to lead with bold ideas, relentless focus, and drive to end the diagnostic odyssey.  Visit www.genedx.com to learn how we’re making precision medicine the global standard of care.  

Summary  

The Associate Variant Scientist performs independent interpretation of DNA sequence and/or copy number variants to support the diagnosis of genetic disease, using both manual and automated methods within a collaborative team environment. Responsibilities include reviewing genomic data across multiple platforms, evaluating pathogenicity of variants, and documenting findings with clarity and precision for downstream reporting. With a focus on analytical accuracy, professional judgment, and adherence to established procedures, the Associate Variant Scientist contributes to high-quality patient care and supports departmental goals through expert variant assessment and process reliability. 

Work Schedule: Tues-Sat 2-10pm OR Sun-Thurs 2-10pm.

Job Responsibilities 

  • Evaluates and assesses the pathogenicity of DNA sequence variants (SNV) and/or copy number variations (CNVs) using approved standard operating procedures (SOPs) and established guidelines (e.g., ACMG/AMP), seeking guidance for complex or novel cases.
  • Reviews genomic data from multiple platforms (e.g., Sanger sequencing, next-generation sequencing, whole exome/genome sequencing, exon microarray, MLPA, qPCR, genome microarray) and completes case-level analysis with minimal supervision.
  • Prepares clear, accurate, and complete documentation of findings for downstream reporting.
  • Maintains high accuracy and meets workload targets while demonstrating growing proficiency in internal systems and tools used for variant analysis and documentation.
  • Meets or exceeds productivity standards as assigned by team lead.
  • Participates in continuing education and stays informed about emerging guidelines and best practices in variant interpretation.
  • May assist with training activities by cross-checking cases or providing informal feedback to trainees under guidance.
  • May assemble, edit, and review genetic test reports, perform data analysis and case management, and/or conduct clinical analysis of genomic data.
  • Performs other duties as assigned to support the team or department.

Education, Experience, and Skills 

  • PhD in medical technology, chemical, or biological sciences.
  • Demonstrated ability to produce high-quality, error-free work across core responsibilities.
  • Proven ability to work independently and collaboratively, with strong verbal and written communication skills and high proficiency in Microsoft Office 365 applications. 
  • Demonstrated professional-level proficiency in mathematical reasoning, computer literacy, and language-based communication.
  • Foundational knowledge or about Variant Science preferred but not required. 

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, 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%).

#LI-REMOTE

Pay Transparency, Budgeted Range
$80,000$100,000 USD

~

Science - Minded, Patient - Focused. 

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. 

With hundreds of genetic counselors, MD/PhD scientists, and clinical and molecular genomics specialists on staff, we are the industry’s genetic testing experts and proud of it. We share the same goal as healthcare providers, patients, and families: to provide clear, accurate, and meaningful answers we all can trust.

SEQUENCING HAS THE POWER TO SOLVE DIAGNOSTIC CHALLENGES.

From sequencing to reporting and beyond, our technical and clinical experts are providing guidance every step of the way:

TECHNICAL EXPERTISE

  • 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.

CLINICAL EXPERTISE

  • Thorough analysis: We classify variants according to our custom adaptation of the most recent guidelines. We then leverage our rich internal database for additional interpretation evidence.
  • Customized care: Our experts review all test results and write reports in a clear, concise, and personalized way. We also include information for research studies in specific clinical situations.
  • Impactful discovery: Our researchers continue working to find answers even after testing is complete. Through both internal research efforts and global collaborations, we have identified and published hundreds of new disease-gene relationships and developed novel tools for genomic data analysis. These efforts ultimately deliver more diagnostic findings to individuals.

Learn more About Us here.

Our Culture

At GeneDx, we are dedicated to cultivating an environment where creativity and innovation thrive. We believe in the power of community and collaboration, where diverse perspectives are embraced, and every voice contributes to our shared success. Our team is a vibrant mix of professionals who challenge and support each other in equal measure, fostering growth both personally and professionally. When you join us, you're not just taking on a job—you're joining a movement. A movement that champions curiosity, embraces change, and believes in making an impact, one patient at a time. Cultural principles we live by:  

  • Be bold in our vision & brave in our execution. 
  • Communicate directly, with empathy. 
  • Do what we say we're going to do.  
  • Be adaptable to change.  
  • Operate with a bias for action.    

Benefits include:

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

GeneDx is an Equal Opportunity Employer.
All privacy policy information can be found here.

Top Skills

Sanger Sequencing,Next-Generation Sequencing (Ngs),Whole Exome Sequencing,Whole Genome Sequencing,Exon Microarray,Genome Microarray,Mlpa,Qpcr,Microsoft Office 365,Acmg/Amp Guidelines,Video Conferencing/Collaboration Tools

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