
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.
🔥 0 minutes ago
🗣️🇪🇸 Spanish Required
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• 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. • Partner with Product, Marketing, and Operations to ensure product-market fit and growth.
• Education: A Master’s or PhD in Human Genetics, Laboratory Medicine, Molecular Biology/Pathology, Life Sciences, or related field. • Expertise: Hands-on experience in clinical genomics workflows, including NGS library preparation, sequencing, and secondary and/or tertiary analysis in a clinical setting. • Technical Knowledge: A solid grasp of variant classification frameworks and a deep understanding of NGS workflows. • Languages: Native in Spanish. Proficiency in English is a must. • Strongly Valued Clinical Experience: Previous background in a hospital or private laboratory setting interpreting NGS patient cases. • Regulatory Knowledge: Familiarity with working in regulated environments, such as IVDR, CLIA/CAP, or similar standards. • Global Mindset: Proven experience in multicultural environments and/or supporting international customers in a scale-up setting.
• 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.
Apply Now🔥 43 minutes ago
Senior Clinical Scientist designing and conducting clinical studies evaluating innovative treatments at ICON. Collaborating on clinical trial protocols and supporting regulatory activities.
🕒 June 17
Manager of Clinical Trial Managers II handling execution of studies and developing a cohesive team environment. Leading a regional team and driving best-in-class day-to-day operations.
🕒 June 9
Senior Clinical Study Manager leading multi-country clinical trials for innovative diabetes management solutions. Overseeing trial quality and performance ensuring regulatory compliance and operational excellence.
🕒 June 5
Clinical Scientist Associate Director at Amgen supporting design, execution, and oversight of global clinical trials. Collaborating with cross-functional teams to deliver high-quality clinical data for regulatory submissions and scientific dissemination.
🇪🇸 Spain – Remote
💵 €90.8k - €122.8k / year
💰 $28.5G Post-IPO Debt on 2022-12
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🕒 June 3
Senior Regulatory Affairs Specialist managing clinical trial regulatory strategies globally for Thermo Fisher Scientific. Leading discussions and providing regulatory advice in a global research context.