Clinical Genomics Scientist II; exome​/genome): REMOTE

Clinical Genomics Scientist II (exome/genome): REMOTE USA

Ambry Genetics

Posted Feb 14

Full-time

Kentucky

Unknown

Compensation
$110,000 - $114,000 per year. You are eligible for a Short-Term Incentive with the target at 5% of your annual earnings; terms and conditions apply.

• Experienced reporting position for individuals, typically genetic counselors or PhD scientists, with clinical laboratory experience. Responsibilities include interpreting diagnostic test results, review and summary of relevant medical literature, and/or review and summary of clinical information.
• The Clinical Genomic Scientist II is highly proficient in variant classification guidelines and in following report generation protocols to meet requirements for quality and turnaround time.
• Has an understanding of genomic technologies and may assist in technical troubleshooting as needed.
• Additional responsibilities as designated by the Supervisor/Manager, which may include providing input in the development of guidelines and/or assisting with training of new Clinical Genomic Scientists.

• Attend and provide input at trainings regarding reporting protocols applicable to the specific position or specialty
• Leverage awareness of current process and systems to provide suggestions for improvements
• Maintain expertise in clinical and technical aspects relevant to the specific position
• Interpret clinical diagnostic testing results in accordance with established SOPs
• Variant assessment and classification
• Independently draft clear, accurate clinical testing results
• Effective communication and collaboration with team colleagues; ability to regularly provide input and receive feedback in team discussions
• Other duties as assigned

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

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