Clinical Research Coordinator
November 28
Description
• Supports the clinical team on multiple clinical studies. • Oversees and coordinates daily operations of the clinical research team. • Prepares and reviews monthly clinical invoicing. • Clinical site support for materials request. • Performs GCP tracking and compliance for multiple clinical studies. • Responsible for the Trial Master File (TMF). • Ensures compliance with SOPs and research protocols. • Tracks and prepares invoicing of clinical milestone payments. • Prepares study documents for clinical site visits in a timely manner. • Assists with IRB and publication. • Follows GCP and GDP to ensure compliance.
Requirements
• Must be extremely detail-oriented • Being proactive is a must for this role • Organized and efficient • Excellent verbal and written communication skills • Multi-tasking is required • Proficient with Microsoft Office programs (i.e., Word, Excel) • A drive to expand knowledge and improve processes
Benefits
• Bonus • Stock
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