Das ist der Job
We offer comprehensive individual development opportunities, continuous trainings, and flexible working hours.
Darum lohnt es sich
Your responsibilities will include Analysis of project data (e.g. trial data) and data processing Statistical programming with SAS and/or R, development of reusable programs (e.g. macros), data visualization, and output generation Specification and creation of (CDISC) analysis datasets Validation of datasets and outputs Support non-clinical / clinical development in all phases Your profile University degree in data science, mathematics, computer science, or equivalent education with a good knowledge in statistics At least three years of experience in SAS programming and clinical research Experience in R programming Excellent working knowledge of clinical trial documents (CSR, SAP, CTR) Very good knowledge of clinical data Knowledge of CDISC standards (ADaM, define.xml, ADRG) Strong analytical and quick-learning skills Knowledge of basic statistical concepts Precise and accurate way of working Team player and a 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.
A modern and bright office with a subsidised canteen, as w
