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: Experience in physical system modelling including finite element modelling Experience working with large codebases in open source software environments Proficient user of HPC environments including MPI
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software such as redcap, R, python. Experience in clinical trial management and coordination, including regulating clinical research with a large human subjects component. Strong knowledge of ICH Guidelines
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meaningful program of work that includes literature reviews, field research, data analysis and scientific writing. The role also involves preparing ethics applications and presenting research findings
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advice and in-depth analysis of complex health data. The role supports both independent and team-based research activities, including the development of manuscripts, conference presentations and funding
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problems, such as phase retrieval or ptychography; and/or (iii) aberration-corrected scanning transmission electron microscope data acquisition and analysis. If you would like to join us in pushing the
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Factors, patient safety, healthcare quality and clinical research or systems improvement; Demonstrated skills in qualitative or mixed methods research, data collection and analysis; and Knowledge of Human
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. About You We’re looking for someone with: An Honours or higher degree in a relevant field Experience in, or strong understanding of, systematic reviews and meta-analysis Familiarity with PRISMA 2020
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and statistics, with expertise spanning time series analysis, Bayesian inference, financial econometrics, and data analytics. As home to one of the strongest forecasting research groups worldwide, we
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: Providing input to grant and proposal writing Literature review Research and Analysis Design Evaluation design and implementation Data Acquisition, analysis, presentation and preparation of a range of
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prototype integration to translate sensor outputs into clinically relevant protein biomarker data. The role will involve laboratory-based experimentation, data analysis, and active contribution to scholarly