593 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "The University of Gothenburg" positions at University of Oxford
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environment, along with excellent organisational and time management skills to manage competing priorities and meet deadlines. You will demonstrate strong attention to detail and accuracy in data entry and
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demonstrable molecular biology skills. You will be able to design the experiments, execute the experiment using various molecular biology techniques, and help analyse the data. You will have highly effective
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it is imperative that samples are promptly received and processed in a timely and rigorous manner, and all data and methodology is recorded in an organised and precise manner electronically
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on patient perspectives and aims to understand the information older people need about the harms and benefits of prostate specific antigen (PSA) testing (ProsDetect II). The second project addresses challenges
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Bath to ensure real-world relevance. The DPhil The specific focus will be refined with the successful candidate. You will use a combination of methods (e.g., systematic reviews, secondary data analyses
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a grant for living costs. Awards are made for the full duration of your fee liability for the agreed course. For more information and details on how to apply please visit the Oxford-Taiwan Graduate
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applications. This will include applying expertise in inorganic polymerisation catalysis and organic functional group chemistry, analysing experimental data, and working closely with project partners. The role
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administrative and data management experience, with the ability to work accurately, paying close attention to detail. You will also have excellent organisational and communication skills and the ability to work
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leadership. Responsibilities include coordinating major research programmes and partnerships, supporting training initiatives such as the Oxford EPSRC Centre for Doctoral Training in Health Data Science
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of human samples collected as part of this clinical trial must comply with the Medicines for Human Use (Clinical Trials) Regulations 2004 and will provide the primary endpoint data that will dictate