Overview In this role you will manage and ensure the integrity of clinical data within PSI's global trial operations. You will collaborate with cross-functional teams to design and validate data capture, lead data quality initiatives, and support regulatory-ready databases. You help drive timely database locks and maintain data management documents, contributing to PSI's mission of high-quality, timely clinical services. This is an opportunity to shape data workflows in a diverse, inclusive environment at a globally active CRO. Benefits * Track database set-up, testing, maintenance and data entry * Communicate with clients, project teams and vendors on data management matters * Review study documents, design and develop project specific guidelines and instructions * Design eCRF, Data Management and Data Validation Plans and test EDC databases * Ensure data entry, follow-up and validation,



including manual CRF review and SAE reconciliation * Code medical data * Track and report metrics leading to database lock * Coordinate the processing, dispatch and archiving of CRFs/queries * Maintain Clinical Data Management working files * Perform database QC checks, prepare and attend audits * Train site staff and project teams on CRF completion and data management topics Responsibilities * Demonstrated experience of managing clinical or medical data * Full working proficiency in English * Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm) * Proficiency in MS Office applications * Organisational and time management skills * Ability to work independently and multi-task Qualifications * Base salary range 34,******,000 gross annual salary * Premio * Incentive plans * Other benefits may apply #J-*****-Ljbffr

📌 Data Manager For Clinical Trials (Bardi)
🏢 Experteer Italy
📍 Bardi