Clinical Data Engineer CDP (Bellprat)

Clinical Data Engineer CDP (Bellprat)

03 oct
|
Bayer
|
Bellprat

03 oct

Bayer

Bellprat

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Clinical Data Engineer CDP & DPMain PurposeDrives 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, ePRO, 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 & ResponsibilitiesRequirements & 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 transfer specifications. Develop and validate programs for study setup, conduct and closeout activities within the Clinical Data Environment/Lakehouse. Provide clinical study data to business users, ensuring smooth data flow and traceability while addressing any data flow issues.
Project Management: Plan, prioritize, and communicate timelines for clinical studies. Support these studies throughout their lifecycle by evaluating issues, assessing the impact of changes, and implementing and testing updates. Ensure all study setup documentation is completed on time and comply with relevant SOPs to be ready for inspec

📌 Clinical Data Engineer CDP (Bellprat)
🏢 Bayer
📍 Bellprat

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