Role Summary
Senior Scientist, Statistical Genetics will apply human genetics to drug discovery and development, performing comprehensive analyses of genetic data to uncover new therapeutic targets with a focus on neurological and ocular diseases. The role leverages biobank-scale data from UK Biobank, All of Us, Our Future Health, the Alliance for Genomic Discovery, and other biobanks. This onsite position is based in Cambridge, MA.
Responsibilities
- Lead target finding and validation efforts for the neuroscience and ocular therapeutic area.
- Apply human genetics (common and rare genetic association studies) using biobank-scale data with the aim of finding new targets for RNAi therapeutics.
- Perform biobank-scale association analyses, conduct meta-analyses across diverse cohorts, and integrate findings with molecular QTLs and other omics data to strengthen hypotheses.
- Perform post-GWAS analyses aimed at identifying causal genes and potential therapeutic targets (e.g., fine-mapping, colocalization, Mendelian Randomization).
- Create and validate new phenotypes including imaging-based phenotypes.
- Collaborate closely with cross-functional teams to follow-up on promising targets and to deliver genetic analyses that will help inform existing drug development programs.
- Stay at the forefront of statistical and computational genetics methods, implementing innovative approaches that accelerate target discovery and validation.
- Communicate findings effectively through internal presentations, project reports, and/or high-impact publications.
Qualifications
- PhD in Statistical Genetics or a related field; 3–6 years of relevant post-graduate experience applying genetics to drug target discovery. Title is commensurate with experience.
- Demonstrated expertise in GWAS and/or RVAS, meta-analysis, and performing post-GWAS analyses to help elucidate causal mechanisms (e.g., fine-mapping, colocalization, TWAS, Mendelian Randomization, polygenic risk prediction).
- Track record using genetic data to make novel biological insights or find new drug targets.
- Deep knowledge of neurological and/or ocular disorders with the ability to contextualize genetics findings into biological mechanisms and clinical relevance.
- Demonstrated experience collaborating with biologists, disease area experts, and physician scientists to interpret the results of genetic analyses, support disease understanding and prioritize follow-up work.
- Well-versed in leveraging publicly available genetics resources (e.g., OpenTargets, OMIM, GTEx, GWAS catalog).
- Proficiency with statistical genetics tools (e.g., PLINK, REGENIE, SKAT) and strong hands-on skills in R and Linux command line.
- Experience working in cloud computational environments for genomics (e.g., UKB RAP, All of Us Researcher Workbench, ICA).
- Independent, detail-oriented scientist with excellent communication skills and a record of publishing impactful research.