Clinical Genomic Scientist II - Exome Analysis (REMOTE:USA)

Compensation:  $105,000 - $118,000 per year. You are eligible to a Short-Term Incentive Plan with the target at 5% of your annual earnings, terms and conditions apply.

Clinical Genomic Scientist II - Exome Analysis (REMOTE:USA)

Job Overview: 

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 Genomics 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 Genomics 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 related 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
• At least 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.
• Must possess strong working knowledge of human genetics and diagnostic genetic testing concepts
• Effective communication and collaboration with team colleagues; ability to regularly provide input and receive feedback in
  team discussions
• 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, …