Staff Product Manager, BioPharma Platforms

atPathAIRemoteUS flagMassachusettsFull-timeProduct ManagerLead$146.3k – $224.3k/year

Posted 6 days ago

This is a fully remote position, open to applicants in Massachusetts.

📋 Description

• Develop and implement a multi-year product strategy, vision, and roadmap for enterprise biopharma platforms that support translational research and clinical development.

• Oversee the entire product development lifecycle, from customer discovery and problem identification to MVP prototyping, PRDs, backlog prioritization, and large-scale enterprise rollouts.

• Collaborate closely with Clinical Operations, Regulatory, Quality, and Data Governance teams to design platforms that adhere to GxP standards, data privacy regulations, and applicable SaMD validation frameworks.

• Create product telemetry, quantitative adoption metrics, and reliability benchmarks.

• Promote best practices in platform product management and provide mentorship to cross-functional team members.

• Advocate for modular and interoperable system architectures.

• Form strategic partnerships with senior scientific leaders and biopharma collaborators to ensure platform investments align 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 field.

• Over 7 years of experience in product management.

• Proven history of conceptualizing, building, and scaling enterprise platforms, data infrastructure, or SaaS products within healthcare.

• Experience in driving software and data products in life sciences, biotechnology, digital health, bioinformatics, or clinical research settings.

• Outstanding communication and influencing skills with technical, scientific, and executive stakeholders.

• Preferred: advanced degree in a relevant field.

• Preferred: experience in delivering MLOps, digital pathology, multi-omics, or regulated clinical trial analytics platforms.

• Preferred: knowledge of regulatory validation and quality compliance, including 21 CFR Part 11, GxP, HIPAA, GDPR, or SaMD.

• Preferred: ability to navigate 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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