Implementation of clinical questions in statistical models and concepts for clinical trials and metaanalysis Responsible biometric planning, including study design, case number planning, protocol development and statistical analysis plan, in particular for randomized clinical studies Participation in the preparation of study reports and study reports Statistical evaluations of clinical studies and the production of biometric final reports in compliance with international guidelines Working in research projects on the application of methods of artificial intelligence, learning algorithms, neural networks, or methods of machine learning in cardiovascular medicine and research Implementation of Big Data Analysis Management of databases and data structuring Creation of database extracts and reports as well as generation, verification and processing of data exports to / from scientific cooperation partners Coordinate medical data systems with regard to data quality and consistency and efficient provision of standardized clinical data Data extraction from clinical primary systems, data preparation and reprocessing, conversions and application of data augmentation techniques Accompanying risk-based, quality-proofing processes in ongoing studies Cooperation with external service providers and partners Coordination of cooperation with senior bodies at the UKB Training of the study staff of the site Cooperation with third-party applications Self-development of study ideas very welcome Participation in investigator meetings and conferences Publication of research results and congress contributions

Successfully completed Master/Diplom study of biostatistics / Statistics / Mathematics or comparable experiences Promotion and/or experience in scientific publications desirable Knowledge gained in the integrated analysis of medical data including advanced statistical methods (complex survival time models, propensity scores and inverse probability weighting, target trial emulation etc.) Experience in dealing with hospital information systems, clinical application systems and interfaces as well as clinical studies desirable Knowledge of mathematical-statistic programming (e.g. R, MATLAB, SPSS, SAS, Python) Knowledge of Big Data Analysis Experience in the management of databases Understanding in the biological/immunological field and interpreting corresponding data Knowledge of the analysis of bioimmunological and multi-omics data and their correlation with clinical results desirable Experiences in the application of methods and tools for the analysis of large data sets (e.g. Next-Generation Sequencing, RNA-Seq, Genomics) desirable Affinity for cardiovascular research field and interest in clinical trials High motivation and commitment as well as the ability to work independently and independently A high level of enthusiasm, organizational talent, communicative characteristics and team skills Very good knowledge of German and English

Responsive and versatile: a workplace with a large design space in a collegial team Payment by TV-L: Tariff compensation incl. Annual special payment (TV-L EG13), occupational pension schemes Flexible for families: flexible working time models, possibility of a place in the farm children's daycare and offers for parental leavers Clever to work: Good connection to the SWB network Supported training: Individual development opportunities through courses, e-learning and coaching Start with system: Structured onboarding Healthy at work: Numerous offers of health promotion, free membership in the UKB gym Benefits: Benefits for employees (Corporate Benefits) We are committed to diversity and equal opportunities. Our aim is to increase the proportion of women in areas where women are underrepresented and to promote their careers in particular. We therefore strongly urge qualified women to apply. Applications are treated in accordance with the National Equality Act. The application of suitable people with proven severe disability and persons with equal status is particularly welcome. .