Studies of Lung Cancer, Melanoma, and Kidney Cancer Using Genomic Data Postdoctoral Fellowship

Specific goals of our research include: Identifying molecular signatures associated with environmental exposures and clinical outcomes; Identifying intra-tumor genetic and epigenetic heterogeneity and tumor evolution; Characterizing the molecular steps that lead from precursor to malignant disease; Identifying rare genetic variants associated with risk of familial melanoma. All studies are large and population-based. We have strong collaborating biostatistics and laboratory teams, and have excellent computing resources for next-generation sequencing and genetic epidemiologic analyses. DCEG fellows have access to data from state-of-the-art studies in cancer genomics and work with highly committed and talented researchers with expertise in epidemiology, biostatistics, and genomics. Learn more about the other advantages of being a DCEG fellow, including our distinctive research environment, mentorship, professional development, compensation and benefits, and commitment to diversity and inclusion.

Applicants with a doctoral degree or background in genetics/genomics, genetic epidemiology, or related field, are encouraged to apply. Experience in analyses of large complex genomic datasets, next-generation sequencing, GWAS, and/or bioinformatics methods is a plus. A successful candidate will have excellent communication skills, be highly motivated and able to work in a large multidisciplinary team. Salary and benefits are highly competitive and commensurate with experience.

U.S. citizens and permanent residents are eligible to apply. NIH welcomes foreign nationals with the exception of individuals from this list.