MapLight Therapeutics, Inc.

Clinical Trial Associate

• Support Clinical Operations and project teams across all phases of clinical projects
• Interact with Clinical teams, site staff, and vendors in the U.S. and worldwide to support project-specific tasks and overall clinical trial management
• Maintain and manage study-system user access and deactivation requests
• Coordinate materials for internal and external meetings
• Distribute safety alerts and relevant documents as required
• Maintain study-team and vendor contact information
• Assist with planning, organizing, and executing study-specific meetings; write and distribute agendas, minutes, and updates
• Review, format, and finalize study-related templates, plans, and manuals as needed
• Assist with maintaining clinical trial insurance
• Route Clinical Research Organization/study-team questions and requests for resolution
• Participate in clinical data review as required
• Maintain complete Trial Master File documentation and conduct ongoing quality and SOP/ICH-GCP compliance reviews
• Route, track, and file Clinical documents
• Review site Clinical regulatory documentation for completeness and dates as needed
• Develop and maintain study-related trackers and analyze or update tracker data
• Support Study Team Leads and Operational Team Leads with other assigned duties

Senior Clinical Trial Associate – Sr. CTA