You will be primarily responsible for all aspects of clinical trials related to statistics in collaboration with clients from academia, hospitals, and industry.
This includes a contribution to study protocols, performing sample size estimations, implementation of randomization schemes, as well as the actual data analysis according to the study protocol and publication of the results.
In addition, you will provide expert support in statistical data analysis to our clients in the field of personalized health and translational research including, but not limited to, inference using generalized linear models, survival analysis or probabilistic outcome prediction.
Internally, you will participate in the evaluation and implementation of new methods to improve existing workflows. The paradigm of reproducible research is of great importance to us.
Therefore, the use of software tools like markdown, git, snakemake, and containers will be required for development and sharing.
You have a PhD in biostatistics or a quantitative science and proven experience in clinical trial statistics. You have profound knowledge of experimental design, broad and deep expertise in applied biostatistics and strong programming skills in R.
Excellent communication skills in English are required, knowledge of German is a plus.