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. The Research Associate will work in close collaboration with the Project Manager, Principal Investigator and all team members. The post holder must have a PhD (or have submitted their thesis) at the time of
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should normally have a PhD (submitted or nearly submitted at the time of application) in a relevant field and with experience of the methods required for this project. They should provide evidence of
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About the role The Department of Social Policy and Intervention wishes to appoint three part-time Research Assistants (RAs) to work on a project related to economic and social inequality in high
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of how alternative land management practices impact greenhouse-gas fluxes through the development and application of sophisticated modelling tools. The work will involve model development on the Cambridge
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About the role The Department of Social Policy and Intervention wishes to appoint three part-time Research Assistants (RAs) to work on a project related to economic and social inequality in high
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-resolved plasma measurements. Responsibilities will include writing refereed publications, managing an industrial research project, and delivering reports to industrial partners. You will join a currently
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publications, managing an industrial research project, and delivering reports to industrial partners. You will join a currently running industry-funded project. The project focuses on the development
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publications and research proposals as well as help manage and direct this complex and challenging project as opportunities allow. Main Duties and Responsibilities Perform the following activities in conjunction
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The Medicines And Healthcare Products Regulatory Agency; | Canary Wharf, England | United Kingdom | 9 days ago
of CPRD's interventional research services. Responsibilities include defining the strategy and implementing standard methods and algorithmic approaches to data capture, transformation and export; undertaking
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+ Clinical Lecturer for a preparatory ‘run-in’ period of up to 12 months before beginning the 3-year PhD project, when clinical training (80%) is combined with protected research time (20%) for selecting