Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full‑service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high‑quality, timely services across a broad spectrum of therapeutic indications.Job Details
- Full‑time
- Milan, Lombardy, Italy
- Posted 2 days ago
Job Description Clinical Data Manager plays a critical role in the clinical research project. If you are detail‑oriented, committed to quality and able to work with large volumes of clinical or medical data, you might be the professional we are looking for.
Responsibilities
- 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
Qualifications
- College/University degree (Life Science, Pharmacy degree is a plus)
- Demonstrated experience of managing clinical or medical data in a CRO is a must
- 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
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📌 Data Manager For Clinical Trials (Italia)
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