Das ist der Job
We offer comprehensive individual development opportunities, continuous training, and flexible working hours.
Darum lohnt es sich
Responsibilities 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, including study planning (protocol, study design), sample size determination, reporting, and analysis plan (e.g., SAP) Customer consulting and direct point of contact Qualifications Master’s degree in statistics, mathematics, or comparable studies; PhD preferred 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 clinical trials Strong 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 a high degree of initiative Good English skills; German is an advantage Benefits We value communication, flat hierarchies, an open corporate culture, and a harmonious work environment.
A modern, bright office with a subsidised canteen, the opportunity to work two days per week from home, and full remote work from anywhere in Germany for those who do not live in Munich can be discussed. You will join an interdisciplinary team that allows you to collaborate with and learn from peers with diverse backgrounds.
Contact If you have any questions, please feel free to contact us by e-mail at application@staburo.de. #J-18808-Ljbffr
