Clinical Scientist

• Interpret and classify genetic variants identified through clinical testing
• Review genomic data from oncology NGS tests and perform somatic variant interpretation
• Evaluate data quality from next-generation sequencing/massively parallel sequencing platforms
• Research clinical significance using medical literature, external databases, and computational prediction software
• Collect and integrate data related to cancer biology and/or heritable disorders and potential clinical-care impact
• Assess plausibility of laboratory results using patient demographics and clinical symptoms
• Draft accurate and consistent clinical reports for medical director review
• Collaborate with laboratory teams, genetic counselors, medical directors, scientists, staff, directors, and management
• Troubleshoot unique scenarios and optimize clinical workflows and processes
• Contribute to quality assurance, standard operating procedures, and best practices for variant interpretation
• Maintain compliance with regulatory standards, policies, procedures, and record keeping
• Accept, resolve, and assist with resolution of problems
• Perform peer assessments as a Qualified Observer after two years of experience
• Maintain current knowledge of genomic research and guidelines
• Spend approximately 85–95% of time analyzing clinical cases

Explore Clinical Variant Scientist I at ARUP Laboratories. Review requirements and application details.

Clinical Variant Scientist I

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