Descripción de la oferta
Clinical Data Engineer CDP & DP Main 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.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. 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. Study Managers, Study Data Managers, Medical Experts, Statisticians, Statistical Programmers, Medical Writing, Drug Safety, Medical Coding) Technology Related Partners: IT System Owners, DSA&I Process Managers/Clinical Data Engineers/Project Managers/Scrum Masters Enabling Functions: External vendors and partner companies Skills & QualificationsEducation: Bachelor's or Master's degree in Natural Sciences, Life Sciences, Statistics, Computer Science, Data Science or related fields. Experience: At least 3 years in a scientific, data-driven position, preferably with experience working in the clinical data management discipline.C#, SQL, SAS, Python, R) and clinical information systems following software development processes.Familiarity with big data technologies, cloud infrastructure (AWS, Azure, GCP), and data integration tools (e.g., Understanding of global regulatory requirements and guidelines (e.g., ICH, GCP, HIPAA) related to clinical investigations and data collection. Knowledge of CDISC clinical data standards. Strong organizational and time management skills, with the ability to work independently and collaboratively in a global environment. Strong communication skills in English, both written and verbal. Application Period:21/09 - 06/10Reference Code:885371 Division:Pharmaceuticals Location:Spain : Cataluña : Barcelona Functional Area:Information Technology Position Grade:VS 1.1 Employment Type:Regular Work Time:Full TimeContact UsAddressTelephoneE-MailAv.
