Clinical Coordinator

Key Responsibilities

• Oversee all aspects of Cofactor Genomics' PREDAPT clinical trial (NCT04510129)
• Ensure regulatory compliance and maintain highest standard for clinical trial management, including monitoring that sites are executing all required activities
• Monitor trial EDC, clinical trial data, and processes
• Create informational materials to provide clinical sites
• Answer logistical and technical questions regarding trial requirements and patient eligibility
• Communicate with clinical sites and vendors to ensure trial success
• Manage on-boarding of new trial sites and site closures
• Create and coordinate monthly communication with clinical trial sites
• Communicate clearly and promptly with all trial stakeholders (written and verbal)
• Coordinate and be directly involved with team on sample procurement initiatives and new site recruitment
• Coordinate with lab on clinical sample pro...