Associate II, TMF Operations - UK - Hybrid
Worldwide Clinical Trials(1 day ago)
About this role
Worldwide Clinical Trials is seeking a Records Management Compliance professional to handle the processing, review, and archiving of essential clinical research documents. The role involves ensuring regulatory compliance and working with electronic document management systems to support clinical trials.
Required Skills
- document Management
- Regulatory Compliance
- Quality Control
- Electronic Document System
- Clinical Research
- ICH GCP
- Data Entry
- Organization
- Microsoft Word
- Microsoft Excel
About Worldwide Clinical Trials
worldwide.comWorldwide Clinical Trials is a top-rated, full-service global CRO. We provide 30+ years of clinical expertise to benefit your study. Learn more about us here.
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