Senior Product Manager

🔥 8 minutes ago

🌐 Brazil, Argentina – Remote

🇧🇷 Brazil – Remote 🇦🇷 Argentina – Remote

⏰ Full Time

🟠 Senior

✅ Product Manager

👻 Ghost score 15%

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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Nacre Capital

WebsiteLinkedInAll Job Openings

11 - 50 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Nacre Capital is a global venture builder that creates, builds, and grows start-ups focused on deep technologies that have a significant societal impact. The company identifies fundamental needs and develops innovative solutions in various sectors, including healthcare, biotechnology, agriculture, and aquaculture. They provide comprehensive support to start-ups, including financial, legal, and recruitment services, and actively help scale their ventures globally. Nacre Capital notably works with companies like FDNA, which assists in identifying rare diseases, and Seed-X, which advances AI-based solutions for seed and grain supply chains.

📋 Description

• Own the product direction and daily product decisions for Family Health Checker and Face2Gene • Define how clinician decision support presents phenotype findings, prioritized genes, syndrome considerations, evidence, and source tags • Develop parent-facing result language, user guidance, consent moments, safety messaging, and escalation instructions • Help develop next-generation visual-AI results, symptom assessment, and health-history features • Design the Family Health Checker-to-Face2Gene handoff and clinician-ready information package • Make Family Health Checker deployable through health-system portals, QR codes, digital front doors, and white-label implementations • Work with engineering and health systems on PDF and structured export, FHIR exchange, single sign-on, and Epic pathways • Plan non-code deployment factors, including invitations, output ownership, privacy and security reviews, and measurable Phase 1 scopes • Configure routing and documentation for pediatrics, developmental pediatrics, genetics, telehealth, testing, and follow-up • Support referral packets, draft medical-necessity letters, ICD-10 support, requisition readiness, and laboratory-ordering integrations • Represent the product in clinical and regulatory reviews, usability testing, and AI model performance gates • Define evidence standards for product claims with AI and validation leadership • Own metrics, instrumentation, event taxonomies, dashboards, and outcome measurement from intake through clinician action • Monitor post-market model alignment, escalation routing, and user experience drift • Engage clinical advisors and design partners and translate feedback into product decisions • Study clinical workflows, audit product screens, identify pathway gaps, deliver product improvements, launch deployments, and establish clinical review processes

🎯 Requirements

• 4+ years in product management, including at least one product owned from definition through to live use with real users • Working knowledge of healthcare; experience building software used in a clinical, diagnostic, or patient-facing setting, or ability to learn a regulated, high-stakes domain quickly • Sound judgment about appropriate software claims • Ability to collaborate with clinical, scientific, or regulatory experts and convert answers into product decisions • Comfort with product prioritization and rejecting unsuitable releases • Familiarity with FHIR and HL7 v2 (recommended) • Experience with major EHRs such as Epic, Oracle Health, or athenahealth in production environments (recommended) • Understanding of health-system rollout stakeholders, security reviews, training, and operational readiness • Understanding of AI calibration, rationale transparency, and training-data limitations • Experience with regulated software quality systems, including design controls, intended use, risk management, human factors, change control, and post-market surveillance • Familiarity with FDA thinking on clinical decision support software and predetermined change control plans • Familiarity with HPO terms, phenotype-driven test selection, letters of medical necessity, and payer documentation • Exposure to genetics, pediatrics, developmental pediatrics, diagnostics, or lab ordering (preferred) • Ability to design workflows to a time budget and evaluate operational costs • Experience owning metric trees and event taxonomies through instrumentation • Track record of managing design partner or clinical advisory groups • Clinical background is welcome but not required; a clinical license/career is not required