Clinical Trial Assistant
Current• Assisted in coordination and management of SAE reporting activities• Assisted in the QC, review, and analysis of clinical data and key study documents• Maintained a moderate level of professional and therapeutic expertise through familiarity with clinical literature• Assisted with development and formatting of documents• Ordered study supplies and oversaw inventory• Prepared and sends study-related documents to CRO, Investigators, etc.• Maintained internal and external study site and vendor rosters• Processed, distributed, and archived central lab reports• Maintained paper and/or electronic study files, as directed• Prepared minutes from project meetings• Supported day-to-day activities of the clinical team, as needed• Arranged on-site and off-site meetings