Senior Scientist Genomics
Listed on 2026-10-01
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Research/Development
Data Scientist, Research Scientist, Clinical Research
Who We Are
Bio Marin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options.
More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world‑class manufacturing capabilities. At the heart of Bio Marin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Worldwide Research and Development
From research and discovery to post‑market clinical development, our R&D engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first‑in‑class and best‑in‑class therapeutics that provide meaningful advances to patients who live with rare diseases.
Senior Scientist, GenomicsLondon ( hybrid role 2 days per week onsite)
Closing date 16th October 2026
We’re looking for a senior scientist to join our Genomics group at Bio Marin.
This role will use human genetics, genomics, real-world evidence, and AI to identify and characterize patient populations, inform clinical and commercial patient‑finding strategies, and support the development of therapies for genetic diseases. The ideal candidate combines strong quantitative genomics expertise with cross‑functional judgment, pragmatism, and the ability to turn incomplete evidence into clear recommendations.Responsibilities
- Carry out analyses that integrate human genetics, literature, EHR/claims data, genetic‑testing data, and other evidence to define disease segments, biomarkers, diagnostic pathways, and patient populations.
- Partner closely with Clinical, Commercial, Real World Evidence, Research, Business Development, and other teams to translate genomic evidence into actionable clinical and commercial recommendations.
- Establish and manage external collaborations with academic investigators, CROs, testing laboratories, and data providers, including defining analytical scope, timelines, deliverables, data needs, and decision criteria.
- Evaluate external cohorts, genetic‑testing laboratories, CROs, and data providers for patient‑identification, prevalence, and genotype‑phenotype analyses.
- Apply statistical genetics, epidemiology, AI/ML, and advanced statistical methods to large‑scale genomic and real‑world datasets; ensure analyses are reproducible, appropriately rigorous, and decision‑oriented.
- Contribute to portfolio prioritization and business development diligence as needed by assessing genetic rationale, patient‑identification feasibility, population size, and data gaps.
- Apply and develop statistical and computational approaches to analyze and interpret whole‑exome and whole‑genome sequence data in combination with phenotypic or other genomic data.
- Communicate recommendations to scientific and non‑scientific stakeholders, clearly distinguishing evidence, assumptions, uncertainty, tradeoffs, and next steps.
- PhD or equivalent experience in human genetics, statistical…
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