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