
501 - 1000 employees
Founded 1999
🧬 Biotechnology
🔬 Science
💰 Series unknown on 2017-11
Biotechnology • Science
Ambry Genetics is a clinical diagnostic laboratory specializing in advanced genetic testing for hereditary cancer, rare disease, and other inherited conditions. The company offers DNA and paired DNA/RNA testing (including +RNAinsight®), exome sequencing with proactive reanalysis (Patient for Life), and lab-supported digital care tools (Ambry CARE) to help identify at-risk patients, facilitate testing, and report actionable results. Ambry also conducts translational genomics research and collaborates with academic and industry partners to improve variant classification and diagnostic yield.
🕒 June 12
🇺🇸 United States – Remote
💵 $110k - $114k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧐 Analyst
🦅 H1B Visa Sponsor
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501 - 1000 employees
Founded 1999
🧬 Biotechnology
🔬 Science
💰 Series unknown on 2017-11
Biotechnology • Science
Ambry Genetics is a clinical diagnostic laboratory specializing in advanced genetic testing for hereditary cancer, rare disease, and other inherited conditions. The company offers DNA and paired DNA/RNA testing (including +RNAinsight®), exome sequencing with proactive reanalysis (Patient for Life), and lab-supported digital care tools (Ambry CARE) to help identify at-risk patients, facilitate testing, and report actionable results. Ambry also conducts translational genomics research and collaborates with academic and industry partners to improve variant classification and diagnostic yield.
• Interpreting diagnostic test results • Review and summary of relevant medical literature • Review and summary of clinical information • Highly proficient in variant classification guidelines • Following report generation protocols to meet requirements for quality and turnaround time • Assisting in technical troubleshooting as needed • Providing input in the development of guidelines • Assisting with training of new Clinical Genomic Scientists
• Ph.D. in Molecular Biology, Genetics, or related scientific field or MS in Genetic Counseling from an accredited institution or MS in Genetics, Molecular Biology, Biochemistry, or other similar field of study • 2+ years of experience in at least one of the following areas: primary genetics literature review, variant classification, genetic evidence summary writing, clinical report drafting, or sequencing result analysis • Thorough and ongoing knowledge of current theories and principles of human genetics • Ability to understand and evaluate genetic data and literature • Excellent written and verbal communication skills • Enthusiasm and ability to work in and contribute to a fast-paced, highly collaborative environment • Familiarity with diagnostic testing methodologies, including next-generation and Sanger sequencing, microarray, and MLPA
• Medical • Dental • Vision • FSA • Paid sick leave • Generous paid time off (PTO) program
Apply Now🕒 June 12
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