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

Ambry Genetics; Aliso Viejo (CA); Remote; USD 105,000 - 110,000; Full time

Job summary

Join a forward-thinking genetics-based healthcare company as a Clinical Genomic Scientist II. This remote position offers an exciting opportunity to interpret diagnostic test results and contribute to the development of genetic testing solutions. You'll leverage your expertise in variant classification and clinical report drafting while collaborating with a dynamic team. Enjoy a supportive environment that values open scientific exchange and fosters professional growth. With a comprehensive benefits program and a commitment to improving health through genetics, this role is perfect for those passionate about making a difference in human health.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

Flexible Spending Account (FSA)

Paid Sick Leave

Generous Paid Time Off (PTO)

Qualifications

• PhD or MS in relevant field with 2+ years of experience in genetics.
• Strong knowledge of human genetics and diagnostic testing concepts.

Responsibilities

• Interpret clinical diagnostic testing results per established SOPs.
• Draft clear and accurate clinical testing results independently.

Skills

Human Genetics

Variant Classification

Clinical Report Drafting

Communication Skills

Genetic Evidence Summary Writing

Sequencing Result Analysis

Education

Ph.D. in Molecular Biology

MS in Genetic Counseling

MS in Genetics

Tools

Next-Generation Sequencing

Sanger Sequencing

Microarray

MLPA

Job description

Compensation: $105,000 - $110,000 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, 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.

About Us:

Ambry Genetics Corporation is a CAP-accredited and CLIA-licensed molecular genetics laboratory based in Aliso Viejo, California. We are a genetics-based healthcare company that is dedicated to open scientific exchange so we can work together to understand and treat all human disease faster.

At Ambry, everyone is welcome. A career at Ambry Genetics is a chance to be part of a dynamic company that aims to improve health by understanding the relationships between genetics and human disease. We earned our reputation as industry leaders by responsibly introducing cutting-edge genetic testing solutions and continually sharing what we learn with the global scientific community.

At Ambry you will be learning, challenging yourself, and having fun while collaborating with teammates through the open exchange of ideas. Our outstanding benefits program includes medical, dental, vision, FSA, paid sick leave and generous paid time off (PTO) program.

Ambry Genetics is an Equal Opportunity Employer (EOE) and we maintain a drug-free work environment.