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Salary
$141k – $211k per year
Location
Remote/Hybrid (San Bruno, United States)
Seniority
Senior · 3+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Verily is Alphabet's life sciences company, established in 2015 out of Google X to apply data science to healthcare. It builds precision health platforms that combine clinical, sensor and genomic data for research studies, chronic care programmes and clinical trial operations. Its work spans software, connected devices and large longitudinal research projects with health systems.

Who We Are

Verily Health is a data platform and technology company purpose-built to power AI-enabled precision health solutions that accelerate research and improve care for individuals and communities. Uniquely positioned at the intersection of technology, data science, and healthcare, Verily transforms multimodal health data into insights, models, and actions that make healthcare more personalized, predictive, and precise.

Description

As a Sightline Product Manager, you will drive day-to-day execution for Verily's flagship population health intelligence platform. This role focuses on commercializing predictive analytics and accelerating our transition into a high-margin data insights business. You will shepherd the platform lifecycle as we scale multi-modal forecasting tools, expand into advanced microbiome sequencing, and capture international markets.

This is an execution-focused position requiring a precise intersection of scientific insight and agile program mastery. Leveraging your background in infectious disease, you will translate complex biological workflows into engineering directives. Using your strong background as a Product Managerand certified Agile practitioner, you will maintain sprint velocities and pipeline tracking to deliver world-class science to our life sciences, biosecurity, and public health partners.

Responsibilities

  • Drive Commercial Product Strategy: Translate complex pharma and biosecurity workflows into clear product requirements and user stories for high-value predictive analytics, forecasting, and variant horizon-scanning tools.

  • Scale Molecular Diagnostic Pipelines: Serve as the core translation layer for engineering and computational biology teams to scale routine digital PCR (ddPCR), amplicon sequencing, and next-generation metagenomic sequencing (mNGS) workflows.

  • Champion Technical Agile Execution: Run daily Scrum ceremonies and own JIRA/Confluence roadmapping from design to production-grade deployment for dedicated software and computational biology squads.

  • Facilitate Ecosystem Integration: Coordinate data integration frameworks across broader public health endpoints and centralized data marketplaces to achieve continuous product parity.

  • Manage Data Governance & IP: Collaborate with clinical, legal, and academic stakeholders to safely navigate complex technical sample transfer protocols, intellectual property, and data licensing guidelines.

Qualifications

Minimum Qualifications

  • Experience:3+ years of demonstrated work experience as a Product Manager, Technical Project Manager, or Technical Product Manager leading platform execution in a life sciences, biotech, or high-tech environment.

  • Educational Background:Degree (B.S., M.S., or Ph.D.) or practical professional experience in Computational Biology, Bioinformatics, Genomics, or a related quantitative life sciences discipline.

  • Domain Expertise:A background in infectious disease (e.g., exposure to epidemiology, molecular diagnostics, public health surveillance, or virology).

  • Technical Operational Depth:Deep familiarity with JIRA ticketing systems, managing data engine deployment cycles, and holding cross-functional squads accountable to delivery timelines.

  • Complex Stakeholder Communication:Proven ability to translate intricate scientific data parameters (such as assay configurations, signal-to-noise ratios, and variant abundances) into structured, scannable technical requirements for platform engineers.

Preferred Qualifications

  • Agile Certification:Active, industry-recognized certification (e.g., CSM, CSPO, PMP-ACP, or SAFe).

  • Direct experience working with high-throughput laboratory data architectures (such as ddPCR data strings, amplicon sequencing, or raw genomic sequence datasets).

  • Familiarity with the biopharma value chain, specifically how population-level biological insights optimize vaccine strain selection and clinical trial recruitment timelines.

The US base salary range for this full-time position is $140,500 - $210,500 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.

Verily Health Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here. If you'd like more information on your EEO rights under the law, please click here.

If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.

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