Nuvisan

TASKS Planning, execution and documentation of statistical analyses for phase I-II clinical trials Input for the study synopsis and study protocol Sample size planning and randomization Creation and review of statistical analysis plans SAS programming and validation of statistical analyses and datasets Input for the study report Preparation of statistical reports Close collaboration with Clinical Data Management, Medical Writing, Project Management and other interdisciplinary departments Ensuring compliance with applicable quality, compliance and regulatory requirements. Creation of SOPs QUALIFICATIONS Completed studies in biostatistics, statistics, mathematics, bioinformatics, epidemiology or a comparable field Professional experience in biostatistics, preferably in the field of clinical trials, in the pharmaceutical industry or at a CRO Excellent knowledge of statistical methods, especially in the evaluation of clinical or observational...