Colorectal cancer progression is driven not only by tumor-intrinsic genetic mutations, but also by how those mutations remodel the surrounding tumor microenvironment (TME) and cell-to-cell communications. This project aims to decipher the complex communication between cancer cells, immune cells, and fibroblasts using a physiological in vivo model. By employing inducible gene-editing technologies combined with optical pooled screens (OPS) and multimodal spatial phenotyping, we seek to understand how specific genetic perturbations allow tumors to manipulate their surroundings. This internship position is located in South San Francisco, on-site. The Opportunity The intern will play a key role in the execution and analysis phase of this study, with a primary focus on processing and integrating high-dimensional sequencing and spatial imaging datasets. Depending on the candidate's background and interest, the role may also include experimental work such as tumor harvesting, tissue sectioning, and library preparation. The expected outcome is a high-resolution spatial map of tumor-immune interactions. The project is estimated to take 3 months, with the possibility of an extension to 6 months for follow-up studies. Program Highlights Intensive 12-weeks, full-time (40 hours per week) paid internship. Program start dates are in May/June 2026. A stipend, based on location, will be provided to help alleviate costs associated with the internship. Ownership of challenging and impactful business-critical projects. Work with some of the most talented people in the biotechnology industry.
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Job Type
Full-time
Career Level
Intern
Education Level
Ph.D. or professional degree