Website Staburo GmbH
Your responsibilities will include
- Analysis of project data (e.g. trial data) and data processing
- Statistical programming with SAS, development of reusable programs (e.g. macros), data visualization, and output generation
- Specification and creation of 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 two years of experience in SAS programming and clinical research
- Excellent working knowledge of clinical trial documents (CSR, SAP, CTR)
- Very good knowledge of clinical data
- Knowledge of CDISC standards (ADaM, define.xml, ADRG) is a plus
- Experience in R programming is a plus
- Strong analytical and quick-learning skills
- Precise and accurate way of working
- Team player and a high degree of initiative
- Good English skills, German is an advantage