
1001 - 5000 funcionários
Na GeneDx, acreditamos que todos merecem cuidados médicos personalizados e direcionados - e tudo começa com um diagnóstico genético. Com um dos maiores conjuntos de dados de doenças raras do mundo, nossos testes de exoma e genoma líderes do setor traduzem dados genômicos complexos em respostas clínicas que desbloqueiam planos de saúde personalizados, aceleram a descoberta de medicamentos e melhoram a eficiência dos sistemas de saúde. Tudo começa com um único teste.
🕒 Abril 15
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

1001 - 5000 funcionários
Na GeneDx, acreditamos que todos merecem cuidados médicos personalizados e direcionados - e tudo começa com um diagnóstico genético. Com um dos maiores conjuntos de dados de doenças raras do mundo, nossos testes de exoma e genoma líderes do setor traduzem dados genômicos complexos em respostas clínicas que desbloqueiam planos de saúde personalizados, aceleram a descoberta de medicamentos e melhoram a eficiência dos sistemas de saúde. Tudo começa com um único teste.
• Supports the interpretation of genetic findings and contributes to accurate diagnosis and case resolution through exome and genome sequencing. • Focuses on learning and applying standard workflows to assist with clinical data analysis, phenotype-genotype correlation, and interpretation of basic clinical features. • Ensures timely documentation, maintains quality standards, and aids departmental initiatives through collaborative engagement and continuous learning. • Performs clinical data analysis and case management to support accurate interpretation of genetic findings. • Establishes phenotype-genotype correlations across a range of genetic disorders. • Investigates and interprets clinical features of genetic conditions using internal resources and professional tools. • Assumes personal responsibility for routine administrative tasks, including reviewing and editing genetic test reports, interpreting variants, and curating internal databases. • Serves as a subject matter expert for designated genes, disorders, tests, and/or workflows. • Participates in client services and communication via email, phone, or other channels to support case resolution and provider engagement. • Performs literature reviews and database searches to support variant interpretation and classification. • May assist with development of variant-, gene-, or disease-specific test information and report language. • Consistently meets or exceeds performance benchmarks. • May abstract clinical information from patient records. • Meets or exceeds productivity and error standards as assigned by team lead. • Performs other duties as assigned in support of the team or department.
• Master’s degree from an accredited genetic counseling program; alternatively, a Master’s or PhD in Biology, Genetics, Biotechnology, or a related field with relevant clinical experience, or an MD/DO with demonstrated expertise in human genetics. • Proven ability to work independently and cross-functionally, with excellent verbal and written communication skills and high proficiency in internal systems and Microsoft Office 365 applications. • Demonstrated professional-level proficiency in mathematical reasoning, computer literacy, and language-based communication. • Comparable educational, clinical, or laboratory experience will be considered, including roles in regulated healthcare or diagnostic environments. • At least one year prior clinical or laboratory experience required. • Prior experience with variant curation is preferred.
• Paid Time Off (PTO) • Health, Dental, Vision and Life insurance • 401k Retirement Savings Plan • Employee Discounts • Voluntary benefits
Candidatar-se🕒 Abril 14
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