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. 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 .