
1001 - 5000 employés
Fondée en 2004
🏥 Santé
🧬 Biotechnologie
⚕️ Assurance santé
Healthcare • Biotechnology • Healthcare Insurance
Natera est un leader mondial de la technologie de tests d'ADN libre circulant, spécialisé dans les tests génétiques non invasifs et les diagnostics. Les solutions innovantes de l'entreprise se concentrent sur des domaines tels que le dépistage prénatal, la détection du cancer et la surveillance des greffes d'organes. En utilisant une bioinformatique avancée et une analyse de l'ADN, Natera fournit aux professionnels de la santé et aux patients des informations cruciales pour prendre des décisions médicales plus éclairées.
🕒 il y a 8 jours
🇺🇸 États-Unis – Télétravail
💵 $180 300 - $230 900 / an
⏰ Temps Plein
🟠 Senior
✅ Responsable Produit
🦅 Parrain de Visa H1B
👻 Score fantôme 0%
🗣️🇺🇸🇬🇧 Anglais requis
D'où vient cette offre
Publiée sur la page carrières de Natera, pas via un site d'emploi
Repérée par Remote Rocketship il y a 8 jours
Toujours ouverte sur le site de Natera. Vérifiée il y a 2 heures.

1001 - 5000 employés
Fondée en 2004
🏥 Santé
🧬 Biotechnologie
⚕️ Assurance santé
Healthcare • Biotechnology • Healthcare Insurance
Natera est un leader mondial de la technologie de tests d'ADN libre circulant, spécialisé dans les tests génétiques non invasifs et les diagnostics. Les solutions innovantes de l'entreprise se concentrent sur des domaines tels que le dépistage prénatal, la détection du cancer et la surveillance des greffes d'organes. En utilisant une bioinformatique avancée et une analyse de l'ADN, Natera fournit aux professionnels de la santé et aux patients des informations cruciales pour prendre des décisions médicales plus éclairées.
• Own the Signatera product strategy and roadmap for hematologic malignancies, beginning with multiple myeloma and lymphomas • Develop and execute the heme product roadmap • Lead market entry planning as a laboratory developed test (LDT), including clinical validation, CLIA and state requirements, reimbursement, payer considerations, and launch readiness • Define product requirements for blood-based malignancies with R&D, Lab Operations, and Software Engineering • Lead product support for clinical trials using Signatera in hematologic oncology, including IUO studies and the path toward IVD and regulated use • Partner with Regulatory, Clinical, and Business Development on trial start-up, study requirements, and companion diagnostic opportunities • Build product performance metrics and dashboards; analyze test volume, adoption, ordering patterns, turnaround time, and retention • Partner with Medical Affairs and Clinical on evidence generation, study design, investigators, trial partners, publications, and congress presentations • Guide development of Signatera Genome in heme, including whole genome sequencing, phased variants, and structural variants • Conduct Voice of Customer interviews, market research, and competitive intelligence • Engage key opinion leaders, advisory boards, and congresses including ASH, EHA, and ASCO • Work with Marketing on positioning, launch plans, pricing, and collateral • Build business cases and financial models • Present strategy, progress, and data-driven recommendations to executive leadership • Perform other duties as assigned
• Bachelor’s degree in life sciences, statistics, engineering, or a related field • 5+ years of experience in product management, product marketing, or market analytics at a diagnostics, biotech, or pharmaceutical company • Working knowledge of oncology molecular testing, next-generation sequencing (NGS), biomarkers, NGS bioinformatic workflows, and genomic data analysis • Experience with data analysis • Experience with clinical trials • Experience in IUO and IVD regulated environments required • Experience bringing a molecular test to market as an LDT, including clinical validation and laboratory requirements • Experience designing or supporting clinical evidence generation • 30–40% travel for advisory boards, congresses, and customer meetings • Understanding of MRD in multiple myeloma and lymphomas • Understanding of somatic variants in whole genome sequencing and MRD tracking • Understanding of LDT market entry requirements and evidence for clinical adoption and payer coverage • Ability to translate customer and clinical needs into product requirements • Strong analytical skills and ability to build metrics, interpret data, and present findings • Basic financial modeling skills • Proficiency with MS Excel, Word, and PowerPoint • Ability to lead without authority and influence cross-functional teams • Strong written and oral communication skills • Ability to explain complex topics simply • Strong customer focus and relationship-building with thought leaders • Strong organization and time management; ability to manage multiple projects and deadlines • Availability during Pacific time hours required • Site-based presence in San Carlos, CA, Boulder, CO, or Austin, TX preferred
• Comprehensive medical, dental, vision, life and disability plans for eligible employees and dependents • Free testing for employees and immediate families • Fertility care benefits • Pregnancy and baby bonding leave • 401(k) benefits • Commuter benefits • Employee referral program • Flexible remote home office / hybrid office setting • Global, diverse and inclusive workplace
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