Jobs / United States / Sanofi US Services INC

Sanofi US Services INC

Senior Principal Scientist/Principal Scientist, Real-World Evidence & Disease Genomics

Cambridge, MA Posted today

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Skills this job asks for

Electronic health recordsStatisticsAgile

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Sponsorship verdict

Sponsorship possible

One solid signal, not two. Worth applying, and worth asking about sponsorship early.

  • Employer is on a government sponsor recordThe US Department of Labor certified 47 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
  • What Sanofi US Services INC paid sponsored hires in similar roles4 certified filings for “Scientist, Disease Data Analytics” (Molecular and Cellular Biologists) in MA: $92k–$135k, median $103k.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Employer is on a government sponsor record
The US Department of Labor certified 47 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. Source: LCA disclosure data (US Department of Labor (OFLC)).
No salary bar for this route
H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
What Sanofi US Services INC paid sponsored hires in similar roles
4 certified filings for “Scientist, Disease Data Analytics” (Molecular and Cellular Biologists) in MA: $92k–$135k, median $103k. Most were filed at wage level II (50%) — 2 lottery entries, ≈31% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).

US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

About the role

Job title:   Senior Principal Scientist/Principal Scientist, Real-World Evidence & Disease Genomics • Location: Cambridge, MA About the Job Join Sanofi's Target, Disease and Systems Biology (TDSB) team and become a key contributor to our Disease Genetics and Genomics cluster. In this role, you will sit at the intersection of real-world evidence generation and disease genomics, leveraging large-scale electronic health records (EHRs) and population biobanks to transform how we understand disease trajectories and evaluate indication expansion opportunities. Working alongside world-class computational and experimental scientists, you will help shape the future of drug discovery and development across Sanofi's therapeutic areas — from early indication prioritization to business development evaluation of external assets.    Within our Disease Genetics and Genomics cluster, you'll play a pivotal role in:    • Developing and applying cutting-edge EHR-based methods, including foundation models and classical statistical approaches, to generate real-world evidence at scale to understand disease trajectories.  • Defining rigorously curated disease cohorts and progression endpoints to support target trial emulation and genomic analyses  • Driving Sanofi's engagement with leading population biobanks, including FinnGen and All of Us, to generate insights with direct impact on R&D strategy    You will operate in an agile, fast-paced environment with access to industry-leading data infrastructure, working in close collaboration with disease area experts, medical teams, and therapeutic program leads to ensure your work translates into tangible impact on patients' lives.    Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In  R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main Responsibilities:   • Lead indication prioritization and expansion for Sanofi R&D assets and external assets by generating target trial emulation from large-scale EHR datasets and biobanks, providing strategic guidance to therapeutic program teams  • Develop and implement methods for the analysis of longitudinal medical records, including classical statistical models and EHR foundation models, to evaluate the impact of drugs on disease trajectories through target trial emulation frameworks  • Define and champion well-curated disease cohorts and disease progression endpoints using EHRs, working in close coordination with disease area and medical expert teams  • Run genome-wide association studies (GWAS) in curated patient cohorts to identify genetic drivers of disease and therapeutic response  • Apply and scale these methods across large population biobanks, including FinnGen and All of Us, to generate robust, reproducible evidence supporting Sanofi's R&D pipeline    About You     Basic Qualifications:     • Ph.D. in Biomedical Informatics, Epidemiology, Computational Biology, Human Genetics, or a related field, with 4+ years of post-PhD experience, preferably in the biopharma or biotech industry  • Excellent knowledge of and hands-on experience working with longitudinal EHR datasets and OMOP common data models  • Knowledge of target trial emulation methods and causal inference frameworks applied to observational data  • Familiarity with GWAS methodology and population-scale genomic analyses  • Good

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