Main Purpose Drives the setup and maintenance of clinical data collection instrument(s), data ingestion and integration capabilities from all study data sources (sites and vendors – labs, IRT, e PRO, digital devices, etc.), based on the Clinical Study Protocol and Medical Standards in collaboration with the study team and other internal as well as external stakeholders.Main Purpose Drives the setup and maintenance of clinical data collection instrument(s), data ingestion and integration capabilities from all study data sources (sites and vendors – labs, IRT, e PRO, digital devices, etc.), based on the Clinical Study Protocol and Medical Standards in collaboration with the study team and other internal as well as external stakeholders.Implements programs/listings for data quality checks as well as builds optimized data flow pipelines to enable risk monitoring processes (CDM,



Med Review, Site Management, Med Coding) and statistical analysis/reporting.Key Tasks & Responsibilities Requirements & Specification: Analyze clinical protocol to create requirements and technical specifications for data collection, data ingestion, quality measures, data integration and transformation for all study sources ensuring complete end-to-end focus. Task Delivery: Setup study level data collection elements as well as program triggers, derivations and data cleaning checks/listings/reports. Setup and perform data ingestion activities for CRO and vendor data, data exchanges with internal and external partner systems, as per agreed data

📌 Clinical data engineer cdp (Barcelona)
🏢 Bayer
📍 Barcelona