ph3Overview /h3pIn 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. /ph3Benefits /h3ulliTrack database set-up, testing, maintenance and data entry /liliCommunicate with clients, project teams and vendors on data management matters /liliReview study documents, design and develop project specific guidelines and instructions /liliDesign eCRF, Data Management and Data Validation Plans and test EDC databases /liliEnsure data entry, follow-up and validation,



including manual CRF review and SAE reconciliation /liliCode medical data /liliTrack and report metrics leading to database lock /liliCoordinate the processing, dispatch and archiving of CRFs/queries /liliMaintain Clinical Data Management working files /liliPerform database QC checks, prepare and attend audits /liliTrain site staff and project teams on CRF completion and data management topics /li /ulh3Responsibilities /h3ulliDemonstrated experience of managing clinical or medical data /liliFull working proficiency in English /liliExperience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm) /liliProficiency in MS Office applications /liliOrganisational and time management skills /liliAbility to work independently and multi-task /li /ulh3Qualifications /h3ulliBase salary range 34,000-52,000 gross annual salary /liliBonus /liliIncentive plans /liliOther benefits may apply /li /ul /p #J-18808-Ljbffr

📌 Data Manager for Clinical Trials (Cusano Milanino)
🏢 Experteer Italy
📍 Cusano Milanino