Clinical Genomic Scientist II, Genome Analyst

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $110k - $114k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧐 Analyst

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Ambry Genetics

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1999

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

💰 Series unknown on 2017-11

Healthcare • Consulting • Biotechnology

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.

📋 Description

• Interpret clinical diagnostic testing results in accordance with established SOPs • Assess and classify variants • Independently draft clear, accurate clinical testing results • Review and summarize relevant medical literature and clinical information • Follow variant classification guidelines and report generation protocols to meet quality and turnaround-time requirements • Attend and provide input at trainings regarding reporting protocols • Suggest process and systems improvements • Maintain expertise in relevant clinical and technical aspects • Communicate and collaborate with team colleagues, regularly providing input and receiving feedback in team discussions • Assist with technical troubleshooting as needed • Provide input into guideline development and assist with training new Clinical Genomic Scientists • Communicate with internal departments to resolve or escalate issues • Perform other duties as assigned

🎯 Requirements

• 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 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 • Maintain expertise in clinical and technical aspects related to the specific position and communicate with other internal departments to resolve/escalate issues as appropriate • Strong working knowledge of human genetics and diagnostic genetic testing concepts