Description
Death is our only foe.
Blueprint was founded by Bryan Johnson, who has the world’s best comprehensive biomarkers. He is quantitatively the healthiest person on the planet.
Blueprint is methodically built on science. Bryan freely shares his protocol, learnings and data with everyone to use. Blueprint has also developed a family of nutritional products to make the benefits of the Blueprint protocol affordable and available to all.
We’re a small, tight-knit team working to clean up the global food supply, provide healthy food to everyone, and build Don’t Die into the most influential ideology in the world. We move quickly, work efficiently, and enjoy an environment defined by competence.
Blueprint is building a measurement-first system for human health. We need a builder with a strong science acumen to own our biomarker strategy end-to-end, from selecting assays and partners to turning longitudinal, high-precision multi-omics into decisions, products, and proof.
Requirements
What you’ll own:
- Strategy: Define the biomarker roadmap across all major ’omics (methylation/epigenomics, RNA/transcriptomics, proteomics, metabolomics) with high precision and repeatability over time.
- Partnerships: Source, vet, and negotiate with labs/CROs/platforms (CLIA/CAP, research-grade), set SLAs, QC bars, batch schedules, and data contracts.
- Assay selection & validation: Choose platforms (e.g., EPIC/WGBS, RNA-seq, Olink/SomaScan, targeted LC-MS/GC-MS, as well as emerging tech) and design validation plans (replicates, spike-ins, controls, precision/accuracy, LOD/LOQ).
- Pipelines & analytics: Stand up ingestion/QC/normalization pipelines; build longitudinal models (mixed-effects, time-series) to detect true within-person change.
- Bioinformatics → product: Translate signals into deployable metrics (risk, trend, response) that power protocols, content, and customer experiences.
- Study design & compliance: Architect IRB-appropriate protocols; ensure data governance (HIPAA/PHI), CAP/CLIA awareness for claims, and auditable methods.
- Cross-functional leadership: Partner with departments and stakeholders to turn evidence into clear, defensible narratives and user experiences.
- Reporting: Oversee the design, improvement, and maintenance of a biomarker performance dashboard (assay QC, turnaround, failure rates, cost per insight) and a living evidence dossier.
You’re great at:
- Practical execution. Strengths/limits, QC levers, and cost/throughput trade-offs across epigenetics, transcriptomics, proteomics, metabolomics.
- All-omics fluency & aging clocks. Comfortable with proteomics, DNA methylation, transcriptomics, metabolomics—and how they power biological aging clocks and complementary biomarker panels.
- Design and User Experience Intuitions. You pick the right tool (mixed models, causal graphs, simple rules) matched to data quality and claim risk.
- Partner management. You’ve scaled with external labs and enforce SLAs and data standards without slowing progress.
- Biomarker platforms & network. Deep hands-on knowledge of existing and emerging measurement systems (lab and device) and a strong partner network across the space.
- Large-scale data, ML & AI. You’ve cleaned, modeled, and interpreted big datasets end-to-end, applying machine learning to extract stable, decision-ready signals.
- Consumer biomarker systems. You’ve built, maintained, or overseen consumer-facing biomarker pipelines and interfaces, turning complex science into clear, reliable user metrics.
- Clinical data expertise. Experienced with large clinical datasets—analysis, interpretation, and presentation—translating results for technical teams, clinicians, and executives.
Qualifications:
- PhD or MS in bioinformatics, computational biology, systems biology, data science, or related field.
- 6–10+ years designing and managing/running multi-omics projects (industry/startup or leading academic core).
- Hands-on with: Python/R, SQL; pipeline tooling; cloud warehousing, data storage and processing; Git & containers.
- Familiarity with CLIA/CAP contexts, HIPAA/PHI, and evidence standards for consumer-facing health claims.
- Excellent communicator who moves smoothly from technical memos to exec-level decisions.
Benefits
Base Salary: $130-250k