The Broad Institute of MIT and Harvard is a leading, world-renowned research organization that pioneers new ways to treat and prevent disease. Our dynamic team, comprising a diverse community of researchers and scientists, is at the forefront of genomic medicine and data analysis, always pushing the boundaries of what is possible in biomedical research. You will contribute to projects of global significance and have the opportunity to showcase your work as many of our projects are open-source. We offer a comprehensive benefits package and flexible remote work setting, fostering an inclusive environment. If you're excited about working on groundbreaking projects and making a real-world impact, come join us!
Data Engineer: We need a skilled Data Engineer to design, build, and maintain data pipelines for storing/querying very large genomic datasets. You'll be instrumental in devising an ecosystem that supports a growing number of projects, annotations, and dataset types. You will create data models and processing graphs, writing scalable CI/CD data pipelines, and work with a friendly and committed team of researchers and engineers (https://docs.google.com/document/d/1m4qRbB1thhnsMFXxDLtQRGOA...). To apply, email Matt (msolomon@broadinstitute.org) with a resume.
Associate Software Engineer: We're looking for an Associate Software Engineer focused on frontend development. You'll be involved in developing the next generation of web applications for visualizing genetic association results. You'll work with leading researchers in disease areas like schizophrenia, bipolar disorder, and inflammatory bowel disease. Your contributions will play a critical role in our understanding of complex diseases (https://docs.google.com/document/d/1eqt-FtiNj1qwu9HpkImrZROc...). To apply, email Matt (msolomon@broadinstitute.org) with a resume.
Software Engineer: You'll be involved in developing the seqr platform which is used by an international consortium of collaborating clinicians, researchers, and industry partners, to significantly improve their ability to search through large genomic datasets and make discoveries and diagnoses. seqr is core to our efforts both in the Rare Genomes Project and the Broad Center for Mendelian Genomics, and has already enabled us to provide genetic diagnoses to more than 2,000 rare disease families. We are now looking for a full-stack software engineer that will help with the next phase of this project (https://docs.google.com/document/d/16Byq42oUSIIpDomIhy9XIyHs...). To apply, email Larry (lbabb@broadinstitute.org) with a resume.