Clinical Trial Associate (CTA)

Responsibilities

• Perform administrative tasks to support clinical trial execution including but not limited to assisting with the development, maintenance, and formatting of documents, review and reconciliation of study-specific information, set up and coordination of meetings, authoring and distribution of meeting minutes, maintenance of study team lists
• Filing of study documents in the electronic Trial Master File (TMF), maintain essential documents lists, participation and coordination of TMF completeness reviews, and may serve as the main study contact for Records Management Track
• Maintain and ensure accuracy of study-specific information and dashboards utilizing databases, spreadsheets, and other tools including CTMS system
• Support tracking of information between the study team, study sites, and specified vendors, including the CRO, and may communicate with these vendors for defined tasks
• Serve as the main study contact for Records Management Track

Requirements

• Bachelor’s degree or equivalent curriculum required; preferably in a scientific or healthcare discipline
• No previous experience required, although relevant research experience is recommended
• Must have the ability to build and maintain positive relationships with management and peers