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11 дней назад

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

148 500 - 214 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Текст:
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TL;DR
Senior Principal Scientist/Principal Scientist, Real-World Evidence & Disease Genomics (EHR/Genomics): Developing real-world evidence methods from large-scale electronic health records and population biobanks with an accent on disease trajectories, target trial emulation, and genomic analyses. Focus on defining disease cohorts and progression endpoints, running GWAS, and building scalable, reproducible pipelines that inform indication prioritization and drug development decisions.

Location: Cambridge, Massachusetts, United States; onsite

Salary: $148,500–$214,500 per year

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines across therapeutic areas.

What you will do

  • Lead indication prioritization and expansion for internal and external R&D assets using large-scale EHR datasets and population biobanks.
  • Develop longitudinal medical-record analysis methods, including classical statistical models and EHR foundation models.
  • Define disease cohorts and progression endpoints for target trial emulation and genomic analyses.
  • Run genome-wide association studies in curated patient cohorts to identify genetic drivers of disease and therapeutic response.
  • Scale reproducible methods across biobanks including FinnGen and All of Us to support R&D strategy.
  • Collaborate with disease experts, medical teams, clinical development, translational medicine, therapeutic program leads, and business development.

Requirements

  • Ph.D. in Biomedical Informatics, Epidemiology, Computational Biology, Human Genetics, or a related field, plus 4+ years of post-Ph.D. experience.
  • Hands-on experience with longitudinal EHR datasets and OMOP common data models.
  • Knowledge of target trial emulation, causal inference, GWAS, and population-scale genomic analysis.
  • Strong coding skills and experience with AI-assisted coding tools such as Cursor or Claude Code.
  • Experience with large biobanks, Trusted Research Environments, or cloud platforms such as AWS and GCP.
  • Ability to develop scalable analytical pipelines and communicate findings to scientific and non-scientific stakeholders.

Nice to have

  • Experience in the biopharma or biotech industry.
  • Experience with agentic AI frameworks for biomedical data analysis or workflow automation.
  • Experience working with UK Biobank in addition to FinnGen or All of Us.

Culture & Benefits

  • Agile, fast-paced environment with industry-leading data infrastructure.
  • Opportunities for career growth through promotion or lateral moves.
  • Employee rewards and benefits programs.
  • Healthcare, prevention, and wellness benefits.
  • At least 14 weeks of gender-neutral parental leave.
  • Patient-informed drug development and access to AI, data, and digital platforms.

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