Senior Product Manager
Caris Life Sciences
August 25, 2026
Remote friendly (Irving, TX)
United States
Marketing
Job Responsibilities:
- Own strategy and a rolling roadmap for an assigned clinical software product; build a sequenced, value-ordered backlog.
- Drive continuous discovery with ordering physicians, pathologists, geneticists, lab operations, and commercial teams; validate problems before committing to roadmap.
- Write product requirements (epics, user stories, acceptance criteria) suited for engineering and regulated environments.
- Define releases (minimum viable scope, launch-readiness criteria) and make go/no-go decisions with engineering, quality, and regulatory teams.
- Own post-launch outcomes: define adoption/utilization/outcome measures, partner with engineering to instrument them, and iterate or retire capabilities based on evidence.
- Facilitate cross-stakeholder working sessions and make trade-offs and priorities defensible.
- Build investment cases for features, technical debt, and regulatory changes.
- Incorporate SOX and FDA change-control obligations into product plans from the start.
- Use generative AI in discovery synthesis, analysis, requirements drafting, and product documentation.
- Prioritize automation of recurring manual workflow steps; measure manual touches removed.
Required Qualifications:
- Bachelor’s degree (Business, CS, Engineering, Health Informatics, or related) or equivalent experience.
- 8+ years product management (or equivalent leadership) with ownership of technical/platform-scoped work.
- End-to-end ownership of a live software product.
- Proven track record writing structured PRDs (epics, user stories, acceptance criteria).
- Experience defining and tracking adoption/utilization/outcome metrics.
- Experience aligning clinical, operational, commercial, and technical stakeholders.
- Fluency with generative AI tools for product work.
Preferred Qualifications:
- MBA or advanced degree.
- Experience in healthcare diagnostics/molecular pathology/clinical laboratory/life sciences software.
- Experience with FDA, SOX, CLIA, or HIPAA environments.
- Ability to translate regulatory constraints into actionable requirements.
- Experience taking new/major products from concept to launch.
- Agile delivery/framework and product-tooling familiarity.
- Strong written and verbal communication with mixed technical/clinical audiences.
- Own strategy and a rolling roadmap for an assigned clinical software product; build a sequenced, value-ordered backlog.
- Drive continuous discovery with ordering physicians, pathologists, geneticists, lab operations, and commercial teams; validate problems before committing to roadmap.
- Write product requirements (epics, user stories, acceptance criteria) suited for engineering and regulated environments.
- Define releases (minimum viable scope, launch-readiness criteria) and make go/no-go decisions with engineering, quality, and regulatory teams.
- Own post-launch outcomes: define adoption/utilization/outcome measures, partner with engineering to instrument them, and iterate or retire capabilities based on evidence.
- Facilitate cross-stakeholder working sessions and make trade-offs and priorities defensible.
- Build investment cases for features, technical debt, and regulatory changes.
- Incorporate SOX and FDA change-control obligations into product plans from the start.
- Use generative AI in discovery synthesis, analysis, requirements drafting, and product documentation.
- Prioritize automation of recurring manual workflow steps; measure manual touches removed.
Required Qualifications:
- Bachelor’s degree (Business, CS, Engineering, Health Informatics, or related) or equivalent experience.
- 8+ years product management (or equivalent leadership) with ownership of technical/platform-scoped work.
- End-to-end ownership of a live software product.
- Proven track record writing structured PRDs (epics, user stories, acceptance criteria).
- Experience defining and tracking adoption/utilization/outcome metrics.
- Experience aligning clinical, operational, commercial, and technical stakeholders.
- Fluency with generative AI tools for product work.
Preferred Qualifications:
- MBA or advanced degree.
- Experience in healthcare diagnostics/molecular pathology/clinical laboratory/life sciences software.
- Experience with FDA, SOX, CLIA, or HIPAA environments.
- Ability to translate regulatory constraints into actionable requirements.
- Experience taking new/major products from concept to launch.
- Agile delivery/framework and product-tooling familiarity.
- Strong written and verbal communication with mixed technical/clinical audiences.