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Job i Aalborg

Do you want to work with standardising data in clinical trial? Are you looking to make significant contributions to securing the success of Clinical Trials (CT)? Would you like to ensure that the collected clinical trial data is meaningful from a scientific perspective? If you are eager to develop and maintain data standards in CT, this presents an ideal opportunity to actively contribute to our ever-evolving data science community. Don't hesitate—apply today and join us in making a difference! The position The position offers a unique opportunity to expand your experience through working in multi-functional and international teams on a variety of clinical and technical projects that span several functions in the drug development value chain. As a member of our team, you will have a diverse set of responsibilities that revolve around the development and use of data standards to support the efficient execution of our global clinical studies. Your responsibilities can be broadly grouped as follows:

  • Define and develop clinical data standards that are compliant with requirements from regulatory agencies (e.g. CDISC, ICH), cater to the operational and scientific requirements in our studies, and support in their continuous improvement
  • Research and engage in external and internal industry best practices in clinical study management to identify and implement improvements and provide expert advice to the organisation in the business processes we ope...