Jobs / United States / Pathai INC
Staff Product Manager, BioPharma Platforms
Pathai INC · 🇺🇸 Boston, MA or Remote · Remote
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 13 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 5 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Pathai INC paid sponsored hires in similar roles1 certified filing for “Product Manager, AI Products” (Computer and Information Systems Managers) in MA: $146k–$146k, median $146k. Most were filed at wage level I (100%) — 1 lottery entry, ≈15% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Pathai INC
The US Department of Labor certified 13 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 5 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Pathai INC →
About the role
PathAI's mission is to improve patient outcomes with AI-powered pathology. Our platform promises substantial improvements to the accuracy of diagnosis and the efficacy of treatment of diseases like cancer, leveraging modern approaches in machine learning and artificial intelligence. We have a track record of success in deploying AI algorithms for histopathology in translational research, pathology labs and clinical trials. Rigorous science and careful analysis is critical to the success of everything we do. Our team, composed of diverse employees with a wide range of backgrounds and experiences, is passionate about solving challenging problems and making a huge impact on patient outcomes. As a Staff Product Manager, Biopharma Platforms, you will shape and drive the core digital platforms that power clinical development and translational research pipelines. In this high-impact strategic role, you will bridge cutting-edge cloud software engineering, clinical trials, machine learning, and clinical research, transforming clinical workflows into seamless, scalable platform capabilities. You will champion platform product thinking across PathAI, ensuring our engineering and clinical teams and biopharma partners can discover, develop, and deliver transformative therapies with unprecedented velocity. Key responsibilities include: • Define and execute the multi-year product strategy, vision, and roadmap for enterprise biopharma platforms supporting translational research and clinical development • Lead end-to-end product development lifecycles from customer discovery and problem framing through MVP prototyping, technical requirement definition (PRDs), backlog prioritization, and enterprise-scale rollouts. • Collaborate closely with Clinical Operations, Regulatory, Quality, and Data Governance teams to architect platform standards compliant with GxP, data privacy regulations, and Software as a Medical Device (SaMD) validation frameworks where applicable. • Establish product telemetry, quantitative adoption metrics, and reliability benchmarks to measure the velocity, scientific impact, and operational health of platform services. • Champion platform product management best practices, mentoring cross-functional team members and advocating for modular, interoperable system architectures. • Act as the strategic partner to senior scientific leaders and biopharma collaborators, aligning technical platform investments directly with enterprise pipeline milestones and portfolio priorities. Who You Are: (Required) • You hold a Bachelor’s or advanced degree (Master’s/Ph.D.) in Computer Science, Computational Biology, Biomedical Engineering, Life Sciences, or a related discipline. • You possess 7+ years of product management experience, with a track record of conceptualizing, building, and scaling enterprise platforms, data infrastructure, or SaaS products for healthcare. • You bring proven experience driving software and data products within life sciences, biotechnology, digital health, bioinformatics, or clinical research environments. • You are an exceptional communicator and influencer who effortlessly navigates technical, scientific, and executive stakeholders to drive consensus and strategic alignment. Preferred • You have an advanced degree in Computer Science, Computational Biology, Biomedical Engineering, Life Sciences, or a related discipline. • Demonstrated success delivering platforms that support machine learning operations (MLOps), digital pathology, multi-omics, or regulated clinical trial analytics. • Practical understanding of regulatory validation and quality compliance in biopharma or diagnostics (e.g., 21 CFR Part 11, GxP, HIPAA, GDPR, SaMD). • Proven ability to thrive in ambiguous, fast-paced R&D environments whi