Clinical Study Associate Manager

Role: Clinical Study Associate Manager supporting clinical trial delivery within Regeneron's global management team. Responsibilities: oversee regional study planning, vendor management, study documentation, system setup (CTMS, TMF), site activation, recruitment, data quality, budget, and study close-out activities; contribute to risk mitigation, feasibility, and inspection readiness. Requirements: Bachelor's degree, 4+ years in clinical operations, proficiency in trial management systems (EDC, TMF, IVRS), budget awareness, vendor management experience, knowledge of GxP and ICH/GCP guidelines. HighValue: clinical trial management, study documentation, vendor oversight, data quality, budget management; experience with biologics or small molecules is implied but not explicitly stated. WorkSetup: On-site with travel (~25%) in Armonk, NY; Warren, NJ; or Cambridge, MA.