516 data-"https:"-"https:"-"https:"-"https:"-"https:"-"IMEDEA-CSIC-UIB" Fellowship positions in United States
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: · Perform collaborative research with multiple faculty members at ARDMRI on projects involving genomics data analysis using single cell RNA-seq, CHIP-seq/ATAC-seq, spatial transcriptomics, HiC/HiCHIP, RIBO
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 8 hours ago
mathematical ADA model to provide quantitative immunogenicity assessment for therapeutic proteins. This model was constructed using antibody titer data from subjects across 10 clinical trials, with ADA time
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analysis, data simulation and imputation. B) Participate in development and testing statistical methods for admixed human datasets. C) Omics (genome, transcriptome, microbiome, epigenome) data integration
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data. The work will incorporate comparative evolutionary biology using extant plants populations and Herbaria collections. The opening is for a postdoctoral fellow with expertise in one or more of the
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. Additional Qualifications Special Instructions Please email Kara your CV, a short description of your research interests, and contact information for 3 references at kara_mckinley@harvard.edu . Selected
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for finalists. Candidates should submit with their application contact information for two to three references from experts at the ladder faculty ranks or highly accomplished senior researchers from corporations
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to submit the names and contact information for at least two (or up to three) references. We encourage candidates to apply by March 2, 2026, but will continue to review applications for up to 30 days from
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signal processing and both time-series and frequency domain analysis of physiological recordings including ECG and nerve recordings. This data is used to investigate the cardiovascular effects of altered
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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | about 8 hours ago
, there are only animal data to inform the safety in pregnant and lactating women. Pregnancy safety and lactation data are collected predominantly in the post approval setting. The 2007 FDA Amendments Act gave FDA
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products. CDRH provides consumers, patients, caregivers, and providers with understandable and accessible science-based information about products. CDRH facilitates medical device innovation by advancing