Data Manager for Clinical Trials

05 ago - Romano di Lombardia
Experteer Italy

Experteer Overview

In this role you will manage clinical data processes to ensure high-quality, timely trials. You will work within PSI’s global clinical operations to handle data management tasks across studies, collaborating with clients, project teams and vendors. You will design and validate data collection and reporting plans, oversee data entry and reconciliation, and support QA and audits. You will play a key part in driving data integrity and efficiency, using leading CDMS tools to enable database lock. This is a chance to contribute to impactful clinical research within a respected, inclusive CRO.

Retribuzione / 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

Responsabilità
- College/University degree (Life Science, Pharmacy degree is a plus)
- Demonstrated xysqume 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

Requisiti fondamentali
- base salary 34,000–52,000 gross annual salary
- premio
- incentive plans
- other benefits may apply

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