46 data-"https:" "https:" "https:" "https:" "https:" "https:" "Dr" "UCL" "UCL" "UCL" uni jobs at University of Liverpool
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We are seeking to appoint a Terry Wall Fellow (Senior Postdoctoral Research Associate). You will be working with Dr Oleg Karpenkov, Prof. Anna Pratoussevitch and Prof. Victor Goryunov within
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helping to strengthen global alignment. You will be led by Dr Adeniyi Olagunju, Principal Investigator of the Perinatal Pharmacology Group in tandem with CELT GH academic Directors, Professor Andrew Owen
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Adult Social Care Testbed (ASCT) and HealthTech Design Studio (HTDS). You will work under the direction of Dr Will Whittaker to design and implement economic evaluations of health and care technologies
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-distance navigation exhibited by seabirds, the project will capitalise on existing high-resolution GPS tracking and remotely sensed data and develop, collect and analyse new data onboard shearwaters
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and maintaining accurate student records, dealing with large data sets, providing administrative support to key University groups and supporting large scale events. This post is fixed term for 12 months
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culture, microscopy, protein and RNA extraction, in addition to experience with organisation of laboratory research consumables and data/record management. There will be opportunities to acquire new skills
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/documentation and developing systems to improve governance in general, but you will also have a physical presence across the campuses supporting inspections and audits, gathering information, conducting basic
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We are excited to announce an exciting opportunity for a Research Software Engineer (RSE) as part of the research team of Imago, the Imagery Data Service. Imago is one of a set of new data services
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significant element of the work will involve complex and sensitive tasks carried out on behalf of the SCL handling and maintaining confidential records and sensitive information. You will liaise with other
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infectious diseases. Working closely with NHS Trusts, UKHSA and academic partners, you will identify and recruit eligible participants, obtain informed consent, collect longitudinal clinical data, and obtain