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 nonclinical / 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 quicklearning skills
- 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
Wevalue communication flat hierarchies open corporate culture and a harmoniouswork environment. We offer comprehensive individual development opportunitiescontinuous trainings and flexible working hours. A modern and bright officewith a subsidised canteen as well as the opportunity to work 2 daysper week from home are part of our everyday working life. Full remote work fromanywhere in Germany for those who do not live in Munich can be discussed. You will join an interdisciplinary team allowing you to discusswith and learn from peers with many different backgrounds.
Question
If you have any questions please feel free to contact us by email
. About us
Staburo GmbH is a data science company specialized in statistical consulting programming and bioinformatics for healthcare projects. Our core competencies include Clinical Statistics Translational Medicine & Biomarkers Phase I & Pharmacokinetics/Dynamics Data Transparency & Disclosure Services Health Technology Assessment and Bioinformatics. Our customers are international pharmaceutical companies CROs biotech companies and medical device manufacturers. Our steadily growing team supports our clients efficiently from study design to data analysis and finally the disclosing and posting of trial results.