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Clinical Genomics Scientist, Oncology Jobs

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Clinical Genomics Scientist, Oncology
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Join BillionToOne as a Clinical Genomics Scientist in Oncology. Utilize your expertise in somatic variant interpretation (ACMG/AMP) and clinical reporting in Menlo Park. You will analyze genomic data, draft clinical reports, and help shape diagnostic policies for innovative liquid biopsy products...
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United States , Menlo Park
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158401.00 - 179521.00 USD / Year
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BillionToOne
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Until further notice
Explore rewarding Clinical Genomics Scientist, Oncology jobs and discover a career at the forefront of personalized cancer medicine. Professionals in this specialized role serve as critical interpreters of complex genomic data, directly impacting patient care by translating tumor DNA sequencing results into actionable clinical insights. These scientists are the vital link between the raw output of next-generation sequencing (NGS) platforms and the oncologist's treatment decisions, working within diagnostic laboratories, biotech companies, or academic medical centers. The core responsibility of a Clinical Genomics Scientist in oncology is the meticulous analysis and interpretation of somatic (tumor-acquired) genetic variants. This involves evaluating mutations identified in a patient's cancer sample against a vast array of biological and clinical databases. They determine the pathogenicity of variants, assess their clinical significance, and identify potential targeted therapies or clinical trial opportunities based on the latest evidence. A typical day includes deep dives into scientific literature, databases like COSMIC, ClinVar, and OncoKB, and utilizing genome browsers to annotate and classify variants according to established professional guidelines such as those from the ACMG (American College of Medical Genetics and Genomics) and AMP (Association for Molecular Pathology). Beyond variant interpretation, common duties include drafting and reviewing detailed clinical reports that clearly communicate complex findings to treating physicians. These professionals often contribute to the development and refinement of standard operating procedures (SOPs) for interpretation and reporting, ensuring consistency and compliance with regulatory standards. They may also participate in molecular tumor boards, providing genomic expertise to multidisciplinary teams. Furthermore, roles frequently involve collaborating closely with cross-functional partners including laboratory directors, bioinformaticians, research and development teams, and quality assurance to improve assay pipelines and support the development of new oncology products. Typical skills and requirements for Clinical Genomics Scientist, Oncology jobs include an advanced degree (Ph.D. in genetics, genomics, or a related life science, or an M.S. in Genetic Counseling) coupled with hands-on experience in clinical variant interpretation. A strong foundation in cancer biology, molecular pathways, and familiarity with FDA-approved therapies and clinical trial landscapes is essential. Technical proficiency often extends to basic bioinformatics tools for reviewing sequence data (e.g., IGV, BAM file analysis). Success in this field demands exceptional attention to detail, rigorous organizational skills to manage caseloads, and outstanding written and verbal communication abilities to collaborate effectively and explain nuanced genomic concepts. For those passionate about leveraging genomics to fight cancer, Clinical Genomics Scientist, Oncology jobs offer a dynamic and impactful career path where science directly informs and improves patient outcomes.

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