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to submit a CV and cover letter. Further Information You must at all times carry out your responsibilities with due regard to the UKRI: • Code of Conduct • Equality, Diversity and Inclusion policy
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experts; (iv) sharing of code with users/testers to ensure rigorous validation/testing and assessment of TRL, including mapping progress towards: (a) Software as a Service, (b) commercial product
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and regulatory requirements in respect of equality and diversity, data protection, copyright and licensing, security, financial and other University policies, procedures and codes as appropriate
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with legal duties and regulatory requirements in respect of Equality and Diversity, Data Protection, Copyright and Licensing, Security, Financial and other University policies, procedures, codes and
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Regulator Code of Practice) as well as experience maintaining sensitive data to a high standard. Knowledge and understanding of due diligence needs and processes. Excellent IT skills including competence with
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solutions Maintain Critical Systems - Ensure our student services applications are available, functioning optimally, and meeting user needs Develop & Enhance - Produce high-quality, structured code and
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, experience in clinical trials or medical research, familiarity with regulatory standards (e.g. ICH GCP, 21 CFR Part 11), and knowledge of clinical coding systems (e.g. CDISC, ICD) would be an advantage
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will drive continuous improvement through code and automation, using tools such as Puppet, Spack, and GitLab/GitHub repositories to deploy solutions and manage CI/CD pipelines. Whether you are
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delay of transition to turbulence. The methodology of the research is theoretical and numerical, i.e. an existing in-house code will have to be modified. This project offers the unique opportunity
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) as well as Master’s level training in quantitative research methods (or demonstrable comparable skills). You will have the ability to conduct reproducible (using code) analyses using R or Stata