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detailed T-cell phenotyping and functional assays • Conduct mechanistic studies using molecular and cellular immunology techniques • Contribute to data analysis, presentation, and publication
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the opportunity for occasional remote working. For more information about the role please view the further particulars below. If you think you have what we are looking for please apply following the guidance below
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will support planning and approval for projects at FMRIB and OHBA. You will ensure that all studies are carried out according to good clinical practice (GCP) and ethical requirements, and that data
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customer service and the ability to work collaboratively with colleagues. You are IT literate, work carefully and accurately, and show discretion when dealing with sensitive information. Experience working
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cancer. You will play a pivotal role in discovering and validating neoepitopes by analysing immunopeptidomic and genomic sequencing data, as well as interrogating in silico datasets. Working closely with
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assessments for a psychopharmacology study, including 7T MRI scanning, logging and analysing data. The study will require adherence to Good Clinical Practice and liaison with senior researchers as
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, fluorescent microscopy, etc.), as well as extensive experience in quantitative proteomics (both sample preparation and data analysis) is expected. As a postdoctoral researcher, you are expected be able
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of the VR programs. The RA will additionally help to write and administer all ethical approvals for the study, ensuring that information is communicated, logged and up-to-date. While most testing will
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• Uncertainty quantification around LLMs • Constrained optimal experimental design (active learning) • Combining models and combining data / Realistic simulation of clinical trials • Developing
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Statement should include a cover letter and should also clearly describe how you meet each of the selection criteria listed in the job description. Click here for information and advice on writing