Clinical Genetic Scientist (ABGC Board Certified)

GeneDx•Gaithersburg, MD

3d•$105,000 - $120,000•Remote

About The Position

At GeneDx (Nasdaq: WGS), we don’t just diagnose rare disease — 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. We’re looking for a Clinical Genetic Scientist (ABGC board-certified Genetic Counselor) who’s ready to bring clarity to complexity and help shape the future of genomic healthcare. In this role, you’ll interpret exome and genome sequencing data, collaborate across disciplines, and deliver insights that directly impact patient care. This isn’t just a job. It’s a chance to transform lives, challenge the boundaries of diagnostics, and contribute to a mission that matters. 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. 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.

Requirements

Master’s degree in Genetic Counseling from an ACGC accredited program.
ABGC board certification (required).
2+ years of experience in a clinical diagnostics lab preferred.
Strong foundation in genomic testing, including variant interpretation and results disclosure.
Excellent communication, time management, and decision-making skills.

Responsibilities

Decode the rare and the complex: perform clinical data analysis, identifying potentially disease associated variants, by integrating molecular variant assessment with your clinical expertise
Own the case: drive each case forward by transforming complex genomic data into clinically meaningful insights
Collaborate to lead: work closely with geneticists, genetic counselors, molecular biologists, and bioinformaticians.
Push the science forward: contribute to internal knowledge sharing and continuous workflow improvement.
Be part of the conversation: participate in team discussions and provide clinical input on patient level interpretation