Saphetor
51 - 200 employees
Founded 2014
🧬 Biotechnology
🤖 Artificial Intelligence
☁️ SaaS
Biotechnology • Artificial Intelligence • SaaS
Saphetor is a company that develops the VarSome Suite, an AI-driven set of bioinformatics software tools for large-scale human genome (NGS) data analysis and interpretation for research and clinical use. Their offerings include VarSome. com (a community-driven variant knowledge base and search engine), VarSome Premium (a subscription with enhanced annotations and analytics), VarSome Clinical (a CE‑IVDR-certified, HIPAA-compliant clinical platform with automated variant classification), and VarSome API for integration. Saphetor supports clinicians and researchers with automated, standards-based variant interpretation, extensive aggregated genomic resources, and scalable SaaS delivery.
Application Scientist, Clinical Genomics
🔥 0 minutes ago
🗣️🇨🇿 Czech Required
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Saphetor
51 - 200 employees
Founded 2014
🧬 Biotechnology
🤖 Artificial Intelligence
☁️ SaaS
Biotechnology • Artificial Intelligence • SaaS
Saphetor is a company that develops the VarSome Suite, an AI-driven set of bioinformatics software tools for large-scale human genome (NGS) data analysis and interpretation for research and clinical use. Their offerings include VarSome. com (a community-driven variant knowledge base and search engine), VarSome Premium (a subscription with enhanced annotations and analytics), VarSome Clinical (a CE‑IVDR-certified, HIPAA-compliant clinical platform with automated variant classification), and VarSome API for integration. Saphetor supports clinicians and researchers with automated, standards-based variant interpretation, extensive aggregated genomic resources, and scalable SaaS delivery.
📋 Description
• Support customers through their journey with VarSome, from pre-sales discussions and platform onboarding to post-sales support and account management. • Act as the technical “closer” by delivering expert demonstrations that bridge clinical needs with VarSome Premium and Clinical. • Lead onboarding sessions for geneticists and bioinformaticians to ensure rapid “time to value”. • Fine-tune filtering strategies and automation to maximize platform “stickiness”. • Systematically gather power-user feedback to influence the product roadmap and cultivate strategic relationships for conference presentations and the development of technical white papers. • Partner with Product, Marketing, and Operations to ensure product-market fit and growth.
🎯 Requirements
• A Master’s or PhD in Human Genetics, Laboratory Medicine, Molecular Biology/Pathology, Life Sciences, or related field. • Hands-on experience in clinical genomics workflows, including NGS library preparation, sequencing, and secondary and/or tertiary analysis in a clinical setting. • A solid grasp of variant classification frameworks and a deep understanding of NGS workflows. • The ability to simplify complex clinical genomics and bioinformatics concepts for clinicians, laboratory technicians, researchers, and IT professionals. • Native in Czech and proficiency in English is a must. • Previous background in a hospital or private laboratory setting interpreting NGS patient cases is strongly valued. • Familiarity with working in regulated environments, such as IVDR, CLIA/CAP, or similar standards. • Proven experience in multicultural environments and/or supporting international customers in a scale-up setting.
🏖️ Benefits
• A competitive compensation package tailored to your unique expertise and professional background. • A remote-first work environment that promotes a healthy work-life balance. • Endless learning opportunities, while transferring new technologies from academics to clinical practice all over the world.
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