stillingsbetegnelse: Biostatistician for clinical development

jobbeskrivelse:
?Biostatistics and Data Management ?Denmark - Søborg If your expertise and professional interest is founded within statistics, and you want to be a part of Denmark’s largest community of biostatisticians, then we have just the right job for you. In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to product introduction. We ensure medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to uniform global standards, regulations and business ethics. About the department The Biostatistics function in our R&D clinical development organisation currently consists of about 160 statisticians and statistical programmers worldwide. Of these, approximately 100 of us are situated in Denmark, where we are organised in key development project teams of approximately 15 statisticians and statistical programmers that cooperates with our biostatistics affiliates and outsourcing partners as well as stakeholders. The job As Biostatistician you are responsible for planning, coordinating and execution of clinical trials and other tasks within clinical development. As Trial Statistician you will be responsible for giving input to protocols and statistical analyses, analysing and interpreting trial results and handle the day-to-day statistical issues during the course of the trial. Other activities include input to manuscripts, posters, risk management plans and other safety reports. Across your tasks, you will collaborate closely together with other Statisticians, Statistical Programmers and interact in our cross-disciplinary teams. Furthermore, you will be engaged in coordinating and supervising the work of contract houses around the world performing outsourced statistical tasks. Development of methods and processes, as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we of course offer great opportunities for on-going training to ensure the continued competency development of our employees. Qualifications You have a solid theoretical background in statistics corresponding to MSc level, and you bring in-depth understanding of practical statistical problems. If you additionally bring statistical experience within the pharmaceutical industry and/or SAS experience it will be an advantage but it is not a prerequisite to apply. As you will work in an ever-changing and global project environment characterised by many deadlines, you must thrive on handling several challenging tasks in parallel without compromising the quality of your work. This takes energy and the ability to work independently with a curious and proactive attitude – as well a flexible and a positive mind set in order to deliver when time is short and deadlines are closing in. You will naturally also need good collaboration and communication skills including solid English skills, written as spoken. Please notice that applications will be processed as they are received. Research & Development is vital to Novo Nordisk’s continuous growth. Your ambition and passion is therefore essential to achieve our goal of creating better lives for people living with chronic diseases. That is why working here is rewarding for us – and for you. Contact For further information, please contact Susanne Gammelgaard Bøttcher +45 3079 1450 or Tu Duyen Le Thi +45 3079 4554. Deadline 8 September 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse:
Arbejde med matematiske, aktuariske og statistiske metoder og teorier

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark