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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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TL;DR
Senior Principal Scientist/Principal Scientist (Real-World Evidence & Disease Genomics): Developing real-world evidence and disease genomics analyses from longitudinal EHRs and population biobanks with an accent on target trial emulation, disease cohorts, progression endpoints, and GWAS. Focus on applying causal inference, EHR foundation models, scalable pipelines, and agentic AI to guide indication prioritization, drug development, and therapeutic strategy.

Location: Cambridge, MA; onsite. US and Puerto Rico residents only.

Salary: $148,500–$214,500 per year.

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines through immunoscience, data, and digital platforms.

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 methods for longitudinal medical-record analysis, including classical statistical models and EHR foundation models, within target trial emulation frameworks.
  • Define curated disease cohorts and progression endpoints in collaboration with disease-area and medical experts.
  • Run genome-wide association studies in patient cohorts to identify genetic drivers of disease and therapeutic response.
  • Scale reproducible analyses across FinnGen, UK Biobank, All of Us, and other large population biobank platforms.
  • Provide strategic guidance to therapeutic program teams and translate analytical findings into R&D decisions.

Requirements

  • Ph.D. in Biomedical Informatics, Epidemiology, Computational Biology, Human Genetics, or a related field, plus 4+ years of post-Ph.D. experience. Biopharma or biotech experience is preferred.
  • Excellent knowledge of and hands-on experience with longitudinal EHR datasets and OMOP common data models.
  • Knowledge of target trial emulation and causal inference frameworks applied to observational data.
  • Familiarity with GWAS methodology and population-scale genomic analyses.
  • Good knowledge of diseases and medical practices, with the ability to engage with clinical and disease-area experts.
  • Strong coding skills and experience using AI-assisted coding tools such as Cursor or Claude Code.
  • Excellent communication skills, including presenting complex analytical findings to scientific and non-scientific stakeholders and influencing strategic decisions.
  • Experience with large biobank platforms such as FinnGen, UK Biobank, or All of Us; Trusted Research Environments or cloud platforms such as AWS or GCP.
  • Ability to develop scalable, reproducible analytical pipelines for large-scale data processing.
  • Experience collaborating across clinical development, translational medicine, and business development.
  • Experience with agentic AI frameworks applied to biomedical data analysis or workflow automation.
  • Ability to work in an agile, fast-paced environment with evolving priorities and an impact-oriented approach to translating science into R&D decisions.

Culture & Benefits

  • Supportive, future-focused environment with opportunities for promotion or lateral career moves.
  • Rewards package and employee benefit programs.
  • Healthcare, prevention, wellness programs, and at least 14 weeks of gender-neutral parental leave.
  • Patient engagement in drug development and studies designed around real-world needs.
  • Work at the forefront of AI, data, digital platforms, and drug discovery.

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