Clinical Genomic Scientist II – Genome Analyst

🕒 August 6

🇺🇸 United States – Remote

💵 $110k - $114k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧐 Analyst

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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 • Review and summarize relevant medical literature and clinical information • Assess and classify genetic variants • Independently draft clear, accurate clinical testing results • Follow report generation protocols to meet quality and turnaround-time requirements • Attend trainings and provide input regarding reporting protocols • Suggest process and systems improvements • Maintain expertise in clinical and technical aspects relevant to the position • Assist with technical troubleshooting as needed • Provide input into guideline development • Assist with training new Clinical Genomic Scientists • Communicate and collaborate with team colleagues, providing and receiving feedback in team discussions • 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 another similar field • 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 • Ability to work in and contribute to a fast-paced, highly collaborative environment • Familiarity with diagnostic testing methodologies, including next-generation sequencing, Sanger sequencing, microarray, and MLPA • Expertise in clinical and technical aspects related to the specific position • Ability to communicate with internal departments to resolve or escalate issues appropriately • Strong working knowledge of human genetics and diagnostic genetic testing concepts

🏖️ Benefits

• Medical insurance • Dental insurance • Vision insurance • FSA • Paid sick leave • Generous paid time off (PTO) program • 401(k) plan • Accommodation support for disabilities or special needs • Second chance employment consideration