Staff Product Manager, BioPharma Platforms
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Job Description
Staff Product Manager shaping AI-powered platforms for PathAI’s clinical development and translational research workflows. Driving enterprise product strategy, regulated delivery, and biopharma collaboration.
Responsibilities:
- 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 from customer discovery and problem framing through MVP prototyping, PRDs, backlog prioritization, and enterprise-scale rollouts
- Collaborate with Clinical Operations, Regulatory, Quality, and Data Governance teams to architect platforms compliant with GxP, data privacy regulations, and SaMD validation frameworks where applicable
- Establish product telemetry, quantitative adoption metrics, and reliability benchmarks
- Champion platform product management best practices and mentor cross-functional team members
- Advocate for modular, interoperable system architectures
- Partner strategically with senior scientific leaders and biopharma collaborators to align platform investments with enterprise pipeline milestones and portfolio priorities
Requirements:
- Bachelor’s or advanced degree (Master’s/Ph.D.) in Computer Science, Computational Biology, Biomedical Engineering, Life Sciences, or a related discipline
- 7+ years of product management experience
- Track record of conceptualizing, building, and scaling enterprise platforms, data infrastructure, or SaaS products for healthcare
- Experience driving software and data products within life sciences, biotechnology, digital health, bioinformatics, or clinical research environments
- Exceptional communication and influencing abilities across technical, scientific, and executive stakeholders
- Preferred: advanced degree in a related discipline
- Preferred: experience delivering MLOps, digital pathology, multi-omics, or regulated clinical trial analytics platforms
- Preferred: understanding of regulatory validation and quality compliance, including 21 CFR Part 11, GxP, HIPAA, GDPR, or SaMD
- Preferred: ability to work in ambiguous, fast-paced R&D environments while balancing architectural stability with agile delivery
Benefits:
- Relocation benefits are not available for this position
- Equal opportunity employment
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