248 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Fraunhofer Gesellschaft" positions at King's College London in United Kingdom
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blockade by monoclonal antibodies. The post-doc will work in a multi-disciplinary environment, alongside data analysts in a group including PhD students as well as master’s and undergraduate students
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are adhered to. We are particularly interested in candidates with knowledge of IP management software such as Minuet (IP Data Management software used at King’s) and experience completing external IP and
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at the bottom of the next page after you click “Apply Now”. This document will provide information of what criteria will be assessed at each stage of the recruitment process. Further information We pride
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and experience required can be found in the Job Description document, provided at the bottom of the next page after you click “Apply Now”. This document will provide information of what criteria will be
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maximising co-stimulation and their influence on the effectiveness of costimulatory blockade by monoclonal antibodies. The post-doc will work in a multi-disciplinary environment, alongside data analysts in a
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. The post is based at the Ule Regulatory RNA Networks lab at UKDRI Centre at King’s. The lab consists of 8 researchers including PhD students and postdoctoral fellows. For more information, please see the
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qualitative data into biodiversity reporting. Review social and ecological impact assessment practice and co-design a conceptual hybrid metric system aligning the needs of corporate standard-setters with rights
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efficiently, reliably and to a high technical standard. The primary purpose of the role is to provide skilled laboratory support across the project, generating high-quality data in molecular biology and cell
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methodologies to test hypotheses and identify suitable alternatives if technical problems arise as well as select, follow, and present scientific data from a variety of sources. You will contribute to discussions
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, including but not limited to screening and enrolling new participants, scheduling and conducting trial visits, collecting research data in line with study protocols, entry of research data into an online