Clinical Data Standards Specialist

The position

will be based in either Aalborg or Søborg. Qualifications To thrive in this role you: Hold a minimum of a university degree within IT, natural sciences or other field of relevance with post-graduate qualifications preferred Bring strong experience within clinical or scientific research and/or working with data and metadata in clinical studies. Approach tasks with a with a high level of scientific rigor and demonstrate a willingness to continuously upskill yourself. You are fluent in oral and written English. As a person you take responsibility and work independently when required in a fast-paced environment with many stakeholders and parallel projects. You are detail-oriented and take pride in delivering high-quality results and can grasp complex processes and systems. About the department In Novo Nordisk Development, we manage clinical drug development worldwide, ensuring that the process lives up to uniform global requirements, regulations and business ethics while delivering viable products that make a difference to patients and ultimately benefit society. Our department, Data Systems and Standards, is a part of Development and consists of 17 enthusiastic and highly engaged people. Working at Novo Nordisk We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energies us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.