Alto Neuroscience Job Trends

The CTA position is responsible for the support of the study team by creating, distributing, maintaining, and organizing study materials, tools and documents to ensure conduct of clinical trials is in compliance with protocol requirements, SOPs and ICH GCP Guidelines. Additional responsibilities include general administrative support to the Clinical Operations Department. WHAT YOU'LL DO Set up, organize, and maintain clinical study documentation, study level files and overall filing of study-specific documentation Assist in the start-up, management, close-out and reporting of assigned clinical studies Coordination of vendor supplies, tracking of inventory and study materials Participate in vendor User Acceptance Testing (UAT)...

The Manager, Clinical Supply Chain is responsible for planning, execution, and oversight of clinical trial supply activities to ensure uninterrupted, compliant, and cost-effective delivery of investigational products and ancillary materials. This role partners cross-functionally with Clinical Operations, CMC, Quality, Regulatory, and external vendors to support global clinical trials from early-stage through late-stage development. WHAT YOU'LL DO Clinical Supply Planning & Execution Develop and manage clinical supply strategies aligned with clinical trial timelines and enrollment forecasts Create and maintain demand forecasts, supply plans, and inventory strategies for investigational medicinal products (IMPs) and comparators Based on study protocol, design clinical supplies to...