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Clinical Genomics Scientist, Prenatal Jobs

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Clinical Genomics Scientist, Prenatal
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Join BillionToOne as a remote Clinical Genomics Scientist specializing in prenatal testing. Utilize your Ph.D. in Human Genetics and expertise in CFTR, HBB, and HBA genes for variant curation and data analysis. Collaborate with a dedicated team to develop policies and impact patient lives through...
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United States
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126721.00 - 147841.00 USD / Year
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BillionToOne
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Until further notice
Explore rewarding Clinical Genomics Scientist, Prenatal jobs and discover a career at the forefront of reproductive medicine. This specialized profession sits at the critical intersection of advanced genomic science and clinical care, dedicated to ensuring the accuracy and clarity of genetic information for expecting families. Professionals in this role are essential team members within diagnostic laboratories, applying deep scientific expertise to interpret complex genetic data from prenatal screenings, such as non-invasive prenatal testing (NIPT) and carrier screening panels. The core mission of a Prenatal Clinical Genomics Scientist is to analyze and classify genetic variants found in fetal or parental samples. A typical day involves meticulous data review, utilizing a wide array of bioinformatics tools, population databases, and published literature to assess the potential clinical significance of genetic changes. Common responsibilities include conducting comprehensive variant curation, determining if a variant is pathogenic, benign, or of uncertain significance based on established guidelines from bodies like the American College of Medical Genetics and Genomics (ACMG). They draft detailed reports summarizing their evidence-based interpretations, which are then used by laboratory directors and genetic counselors to guide patient consultations. Furthermore, these scientists often contribute to the development and refinement of internal curation protocols and standard operating procedures to uphold the highest standards of laboratory quality. To excel in these jobs, individuals typically possess an advanced degree (Ph.D. or Master’s) in genetics, genomics, molecular biology, or a closely related field. A strong foundation in human Mendelian genetics, particularly concerning inherited conditions commonly screened for in prenatal settings, is paramount. Required skills include proficiency in genomic databases and browsers, exceptional analytical and critical thinking abilities, and a keen attention to detail. Familiarity with clinical guidelines and a commitment to ethical practice in prenatal genetics are essential. Effective written communication skills are also crucial for clear reporting. For scientists passionate about translating complex genomic data into actionable clinical insights that support informed family planning, Clinical Genomics Scientist, Prenatal jobs offer a challenging and profoundly impactful career path. This field is ideal for those who thrive in a rigorous, evidence-based environment and seek to contribute to the vital field of prenatal and reproductive health.

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