Data Management Specialist Overview The Data Management Specialist will join Global Clinical Science department of Menarini Stemline, the R&D organisation of the Menarini Group. As a Data Management Specialist, you will develop and maintain the eCRF and other data collection tools in line with clinical trial protocols, regulatory requirements, and standards (e.g., CDISC/CDASH). You will manage system access, provide guidance for data collection, oversee the process, perform data validation (review, queries, etc.), and generate final standardized datasets (e.g., CDISC/SDTM) suitable for analysis. Main Activities & Responsibilities Responsibility for data management documents of assigned Phase I-III clinical trials; Support, review and supervision of all internal or outsourced data management activities for assigned clinical trials; Main contact for external vendors for all data transmission or data collection, including, but not limited to: external labs, IRT, eCOA; Design of the eCRF; Programming of SDTM datasets; Contribute to maintenance of internal procedures relating to data management activities. Job Requirements Master degree in scientific disciplines (statistical sciences, biology, computer science, mathematics, pharmacy, CTF). Experience of at least 3-5 years in the role of Clinical Data Manager. Fluency in English. In order to perform the role in the best possible way, the necessary technical knowledge required are: Knowledge of CDISC standards (i.e .: CDASH, SDTM); Knowledge of C / C # language; Knowledge of data collection systems (i.e .: eCRF, IRT, eCOA); Knowledge of SAS base; Knowledge of the main guidelines (EMA / FDA). Menarini Stemline is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees