Your responsibilities will include

Analysis of project data (e.g. trial data) and data processing
Statistical programming, development of reusable programs (e.g. functions, macros), data visualization, program validation, output generation
Support non-clinical / clinical development in all phases, study planning (protocol, study design), sample size, reporting, analysis plan (e.g. SAP)
Customer consulting and direct point of contact

Your profile

Master´s degree in statistics, mathematics, or comparable studies or PhD
First professional experience as a statistician with responsibility for clinical studies is an advantage
Very good methodological knowledge of basic and advanced statistical methods in the field of clinical trials
Very good IT skills, especially with statistical analysis tools (SAS, R)
Knowledge of relevant terminology in clinical and non-clinical research
Knowledge of relevant guidelines GCP, ICH
Quick comprehension and analytical thinking
Team player with high degree of initiative
Good English skills, German is an advantage

What we offer you

We value communication, flat hierarchies, open corporate culture, and a harmonious work environment. We offer comprehensive individual development opportunities, continuous trainings, and flexible working hours. A modern and bright office with a subsidised canteen, as well as the opportunity to work 2 days per week from home are part of our everyday working life. Full remote work from anywhere in Germany for those who do not live in Munich can be discussed. You will join an interdisciplinary team allowing you to discuss with and learn from peers with many different backgrounds.

Question?

If you have any questions, please feel free to contact us by e-mail application@staburo.de.