25 structures-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "https:" "https:" "Univ" positions at The University of Southampton
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place in the Faculty of Medicine can be found on the Faculty of Medicine website at https://www.southampton.ac.uk/study/subjects/medicine . You will be involved in module leadership, teaching, curriculum
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the Digital Services application support team who are responsible for the digital services that underpin the work of NIHRCC and also offer support to the School. Further information can be found at: https
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with our four research centres (https://www.southampton.ac.uk/research/areas/psychology ). We particularly welcome applications from candidates whose research can contribute to one or more of our cross
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tissues and (where relevant) soil. The modelling work will be tightly coupled to experimental campaigns and will use image-derived structures (including XCT images where available) to develop mechanistic
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airborne acoustics, air-coupled ultrasonics, structural vibration/waves. Work in specialist facilities including anechoic chambers and controlled experimental environments, ensuring high-quality, repeatable
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variables from medical records into structured formats aligned to the protocol and data dictionaries. Curate, validate and reconcile clinical data with laboratory/biomarker and study datasets; resolve data
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projects that uplift personalised diagnostics through the integration of high‑throughput genomic sequencing data with structured clinical data from electronic health records. Develop, implement and maintain
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to promoting equality for women in science and engineering. Our Faculty offers exceptional research facilities in fluid dynamics, structures, and their interactions. This includes a world-class fluid dynamics
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Grant “Unwrapping topologically protected light on topologically structured surfaces”. Building on the University of Southampton’s long-established and internationally recognised strength in metasurface
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diseases such as lung cancer, asthma, and COPD. Post 3 : Design of modified oligonucleotides to target IRES structures of oncogenic mRNAs, avoiding global translation inhibition and testing efficacy in