Associate

• Coordinate and track project team system access
• Maintain project portals and perform documentation quality checks
• Support preparation, management, and shipment of clinical trial documentation, including Investigator Site Files
• Manage version control and quality review of project documents
• Ensure timely submission of documents to the Trial Master File
• Track key project information, including site communications and medical question logs
• Prepare and distribute meeting minutes for sponsor, project, and internal management meetings
• Maintain site and study personnel records
• Coordinate project-specific training activities and monitor completion
• Contribute to onboarding, coaching, training, and leadership of Clinical Trial Associates
• Support continuous process improvement initiatives
• Collaborate with Project Managers, CRAs, and cross-functional study teams across multiple clinical projects

Explore Senior Clinical Trials Associate at Worldwide Clinical Trials. Review requirements and application details.