Duties and Responsibilities:

  • Cooperation on statistical planning, analysis and reporting of clinical studies in all phases of development.
  • Supervision and collaboration with statistical programmers and data managers.
  • Choice of appropriate statistical methods and their adequate description in statistical analysis plans.
  • Interpretation of statistical results in clinical research reports.
  • Statistical review of study protocols and reports and statistical outputs.
  • Participation in interdisciplinary meetings in English.


  • Academic degree in statistics, mathematics or specialization in quantitative methods in a natural science.
  • Solid methodologic knowledge of statistical methods.
  • Capability and willingness to read and utilize recent statistical literature.
  • Fluency in English, written and spoken.
  • Basic knowledge in the areas of databases, SAS programming and MS Office.
  • Logical thinking, structured, targeted way of working.
  • Interested in cooperating in multidisciplinary, international teams.
  • Previous experience in clinical studies is an advantage, but not a prerequisite.

We Offer:

  • Pleasant working environment within a team of highly motivated specialists.
  • Challenging and versatile tasks in the area of international drug development.
  • Scientific working atmosphere and regular professional training.
  • Professional IT support for the performance of all tasks.
  • Competitive salary.
  • Excellent professional development opportunities in a globally operating company.
  • Thorough training on the entire spectrum of the drug development process and statistical methods in clinical studies for recent graduates.