Clinical Trial Coordinator

Description of Job

DESCRIPTION OF JOB RESPONSIBILITIES:

• Scanning, copying, and filing clinical study documentation into eTMF or equivalent documentation tracking and storage system
• Storage and archiving of study documents for long-term storage
• Administrative support of clinical trials: Review of initial site regulatory documents
• Preparation of Investigational Product orders for clinical studies
• Maintenance of Clinical Database as needed
• Perform light data entry as needed
• Interact with clinical vendor site
• Can be assigned to other equivalent support activities to meet business needs