Clinical Data Specialist

Overview

Clinical Data Specialist position based in Italy (Novara) in a permanent role. Role involves supporting the management, validation, and structuring of clinical and scientific data within research projects, working with complex datasets, ensuring data quality, and contributing to standardized outputs aligned with international guidelines. Responsibilities

Management and analysis of clinical data through extraction, analysis, and manipulation of data from study data collection systems Development of queries and automated checks to ensure data consistency and completeness Data cleaning activities and continuous monitoring of dataset quality Support in the configuration and management of clinical databases and EDC systems Development and implementation of data validation rules and edit checks Management of database changes and support for testing and validation activities Structuring and preparation of clinical datasets in accordance with CDISC standards Integration and consolidation of data from multiple sources Production of datasets ready for analysis and reporting Verification of data consistency and management of discrepancies Support for database lock and data archiving activities Preparation of technical documentation and metadata associated with datasets Qualifications

Bachelor’s or Master’s degree in Life Sciences, Biology, Biomedical disciplines, Engineering, Statistics, Computer Science, or related fields with a strong academic background Experience in the management and processing of clinical or scientific data, preferably in clinical research or biomedical environments Good knowledge of Clinical Data Management processes and applicable regulations in clinical studies Knowledge of CDISC standards, particularly SDTM and ADaM, and clinical dataset structuring principles Experience with SQL or similar tools for querying and manipulating databases Advanced use of Microsoft Excel for managing and analyzing large datasets Experience in data validation, development of edit checks, and query management Familiarity with EDC systems and data extraction and integration processes Strong analytical skills, attention to detail, and ability to work autonomously on complex datasets Nice to Have

Experience in regulated clinical trials and exposure to regulatory submissions Familiarity with data integration pipelines or statistical programming environments Apply now to join Nubilaria and contribute to high-impact clinical data projects. About Nubilaria

Nubilaria delivers high-quality data-driven solutions in regulated environments, supporting clinical research and scientific projects through strong expertise in data management, quality, and compliance. Apply now to be part of Nubilaria’s growth journey. Closing Date:

June 30, 2026 Website/URL for further details:

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