Research Analyst

• Establishes and maintains the Clinical Trial Management System (CTMS) and Trial Master File (TMF) in inspection-ready state
• Communicates with assigned sites to drive collection and review essential documents throughout the study
• Performs QC reviews of study files
• Supports development and maintenance of study documents and templates
• Reviews activities of assigned clinical trials to ensure data integrity and adherence to Federal regulations
• Observes and supports site monitoring visits alongside senior CRAs

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