Clinical Trials Manager, Early Phase

Role: Manage Phase I clinical studies across multiple regions and vendors, ensuring compliance, quality, and alignment with study objectives. Responsibilities: oversee study logistics, budgets, timelines, CRO/vendor interactions, site activities, and regulatory compliance; contribute to study protocols, plans, reports, and process improvements; support training and cross-functional collaboration. Requirements: 5+ years with BS/BA or 3+ years with MS/MA, experience in clinical operations within biopharma; strong knowledge of GCP, FDA/EMA regulations, and study management tools; effective communication and team support skills. Preferred: advanced degrees (MA/MS/PharmD/PhD), experience with multicenter/global studies, vendor management, and working in regulated environments. High-Value: Phase I studies, multi-region/global scope, vendor oversight, regulatory compliance, clinical operations expertise. WorkSetup: not specified; travel may be required.