Clinical Genomic Scientist II (genome analyst): REMOTE, USA

Location: Ambry Headquarters

Time Type: Full time

Job Description

Compensation:

$110,000-$114,000 annually

Clinical Genomics Scientist II - Remote US:

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. The Clinical Genomic Scientist II 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.

Essential Functions:

• 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

Qualifications:

• 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 concept

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