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required; proficiency in Danish or German is an advantage. Work Environment & Research Team The postdoctoral researcher will work closely with Associate Professor Christian Lyhne Ibsen, another postdoc and
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Associate Professor Christian Lyhne Ibsen, another postdoc and an international advisory board, including leading scholars from Harvard University, MIT, Boston University, University of Konstanz, and Stanford
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teamwork with other local consortium members in the capital region of Denmark and with parallel international collaborators in the UK. In addition, collaboration with other NIVI-R human challenge sites will
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Senior Analytical Chemist/Platform Manager in mass spectroscopy and chromatography – LC-MS and GC-MS
at all levels (PhD students, postdocs, and professors at all levels). In addition, the Platform Manager is expected to interact with other related analytical platforms at the department and across
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is a fixed term position for 36 months. Introduction The Postdoc will contribute to the ERC-funded project “Women in the Nordic Enlightenment (WHENCE). Changing the narratives of early modern
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, computational chemistry or similar. Our group and research- and what do we offer? In our group we work with theoretical catalysis, which is based on atomic scale simulations and dynamics. In this way we have
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organising and conducting their own research project (under supervision). The programme culminates in the submission of a PhD thesis, which the student must defend in public. The programme is prescribed to 180
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usually have components in all the disciplines: applied data analysis, development/application of advanced statistical methodology, coding of algorithms and computer simulation, and writing of research
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assistant, you are currently enrolled in an educational program (i.e. an active student), preferably with at least 2 years of study left. We encourage students from any field of study to apply, provided
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of Copenhagen teacher training programme for assistant professors is required. Teaching qualifications in relation to trial methodology, including Good Clinical Practice and General Data Protection Regulation