Product Manager

Offre fantôme probable

🕒 il y a 5 mois

🇩🇪 Allemagne – Télétravail

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

✅ Responsable Produit

👻 Score fantôme 69%

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🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Nucs AI

Nucs AI

1 - 10 employés

🏥 Santé

🤖 Intelligence artificielle

🧬 Biotechnologie

Healthcare • Artificial Intelligence • Biotechnology

Nucs AI, la solution de pointe révolutionnant la gestion clinique du cancer de la prostate. Notre plateforme exploite la puissance de l'intelligence artificielle pour offrir des perspectives inégalées sur les lésions tumorales, permettant à la fois aux patients et aux professionnels de santé de bénéficier d'analyses avancées et d'outils d'aide à la décision basés sur des preuves. Avec Nucs AI, les patients atteints de cancer de la prostate peuvent aborder leur parcours de traitement avec confiance, sachant qu'ils ont accès aux informations les plus complètes et personnalisées disponibles. Notre plateforme fournit des évaluations détaillées des lésions tumorales, permettant aux professionnels de santé d'adapter les plans de traitement aux besoins uniques de chaque individu. En combinant une technologie d'IA de pointe avec un engagement envers les soins aux patients, Nucs AI est à la pointe de la transformation de la gestion du cancer de la prostate. Rejoignez-nous pour façonner l'avenir des soins de santé et améliorer les résultats pour les patients dans le monde entier.

Description

• Own the roadmap for one or more product lines (e.g., DeepPSMA, SelectPSMA, TrackPSMA), balancing clinical impact, technical feasibility, and business value. • Engage directly with clinicians, nuclear medicine physicians, and oncologists to deeply understand their workflows, pain points, and decision-making processes. • Translate ambiguous, technically complex problems into well-structured product requirements and clear success criteria. • Develop and articulate a clear product narrative: why this feature matters, who it serves, and how it connects to the broader platform vision. • Navigate the regulatory landscape (FDA, CE marking) as a stakeholder, you do not need to be a regulatory expert, but you must understand how regulatory requirements shape product decisions and timelines. • Drive cross-functional execution with engineering, AI/ML, clinical, regulatory, and commercial stakeholders, keeping a small team moving fast without sacrificing quality. • Contribute to go-to-market strategy, positioning, and customer enablement alongside commercial and clinical teams. • Define and track meaningful product metrics; use data and user feedback to inform iteration and prioritization decisions.

🎯 Exigences

• 3-6 years of product management experience in a B2B or technical environment building products for specialized, professional users (not purely consumer products). • Demonstrated ability to manage complex products where the user base has deep domain expertise, e.g., enterprise software, developer tools, scientific instruments, industrial platforms, or similar. • Strong conceptual and systems thinking. You can see the big picture, connect disparate inputs into a coherent product thesis, and reason about second-order effects. • Startup or high-growth experience. You have worked in an environment where speed, ambiguity, and wearing multiple hats were the norm, not the exception. • Excellent communication skills. You can write clearly, present a compelling argument, and facilitate productive discussions with both technical and non-technical stakeholders. • Comfort with technical depth. You do not need to write code, but you should be able to engage meaningfully with engineers and data scientists on architecture, data, and tradeoff discussions. • Intellectual curiosity and learning agility. You pick up new domains quickly and enjoy becoming a quasi-expert in areas you previously knew nothing about. • Bonus Points: Experience in healthcare, medtech, health-AI, or a regulated industry. Familiarity with medical imaging, oncology workflows, or clinical decision support. Experience working with AI/ML-driven products where model behavior shapes the user experience. Exposure to FDA 510(k), De Novo, or CE marking processes for software as a medical device (SaMD).

🏖️ Avantages

• Mission with real impact – Your work directly improves how cancer patients are diagnosed and treated. • Ground-floor opportunity – Early-stage company, meaningful equity, and outsized influence on the direction we take. • World-class collaborators – Work alongside leading oncologists, nuclear medicine physicians, and AI researchers globally. • Massive market tailwinds – Radioligand therapy and AI-driven oncology are multi-billion dollar growth markets. • Autonomy and flexibility – Remote-first, flexible working. We hire great people and trust them to deliver. • Equity upside – Competitive equity package. We’re building something big and want you to share in it.

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