
Variant Scientist
Tempus
- Location
- United States of America
- Posted
- Salary Range
- 60k - 100k USD
Variant Scientist job at Tempus, utilizing software tools and clinical expertise to analyze molecular data and generate high-quality reports.
Tempus
Variant Scientist job at Tempus, utilizing software tools and clinical expertise to analyze molecular data and generate high-quality reports.
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Tempus is seeking a Variant Scientist to join their Clinical Teams on patient molecular reports for clinical utility. The role involves accurately classifying somatic and germline variants, utilizing software tools, and summarizing test results. The ideal candidate has a degree in Cancer Genetics or related field, prior experience in diagnostic laboratories, and excellent communication skills. They must be detail-oriented, flexible, and able to work independently and as part of a team. Tempus offers a dynamic work environment with opportunities for growth and development.
Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
We are looking for a Variant Scientist who will work with our Clinical Teams on patient molecular reports for clinical utility.
Responsibilities Include:
Accurately classify somatic and germline variants for liquid biopsy, panel tests, and whole exome NGS sequencing
Utilize a variety of in-house software tools to analyze clinical molecular data
Read and interpret scientific literature and curate relevant findings in a clear, concise, and precise manner
Summarize somatic and inherited genetic test results to generate high quality clinical reports
Perform critical quality control functions for molecular reports that complies with quality management programs and standard operating procedures
Support improvements for current assays and processes
Curate variants, genes, and diseases for scientific and clinical relevance
May train junior team members
Preferred Qualifications:
MS or PhD degree in Cancer Genetics, Human Genetics, or Biological Sciences
Prior experience in a diagnostic laboratory, clinical report writing, and familiarity with human mutation databases, genome browsers, and HGVS nomenclature is preferred. Oncology experience strongly preferred
Must have utmost attention to detail, excellent communication, and writing skills
Ability to accurately follow formal documentation and protocols
Ability to work in both an individual and group setting. Must be flexible and able to adjust priorities according to workload or management needs.
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