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Stellenangebotsbeschreibung: Your responsibilities will include• CRF design• Database design and set-up• Creation of Data Management Plan and Data Validation Plan• User acceptance testing• eCRF completion guideline• Data cleaning, SAE reconciliation, query management• Medical coding (e.g., MedDRA, WHO-DD)• Programming of plausibility checks• Creation of SDTMs, define.xml and cSDRG is an advantageYour profile• University degree in data science, statistics, computer science, or comparable studies• At least two years of professional experience as a data manager with responsibility for clinical studies• Knowledge of CDISC standards (SDTM, define.xml, cSDRG)• Knowledge of relevant terminology in clinical and non-clinical research• Knowledge of relevant guidelines GCP, ICH• Quick comprehension a...