Application Scientist – Clinical Genomics

🕒 July 17

🇵🇱 Poland – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 17%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Saphetor

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2014

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

Healthcare • Consulting • Food & Beverage

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 our 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. • Own the customer evaluation process, solve “pain points” around variant analysis, and advise on lab equipment/system integrations. • Lead onboarding sessions for geneticists and bioinformaticians to ensure rapid “time to value”. • Act as the primary lead for on-premises and private cloud deployments, coordinating infrastructure specifications (storage, network). • Fine-tune filtering strategies and automation to maximize platform “stickiness”. • Systematically gather power-user feedback to influence the product roadmap. • Collaborate 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 Polish. Proficiency in English is a must. • Previous background in a hospital or private laboratory setting interpreting NGS patient cases. • 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 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.