Associate Director, Clinical Operations (Site Operations)

Role: Associate Director, Clinical Operations, providing strategic leadership over site start-up and ongoing site management for late-phase, post-marketing, and real-world studies in biopharma. Responsibilities: oversee site documents, IRB submissions, budgets, safety notifications, study communications, and site closeout; develop and monitor operational metrics; implement best practices; support team development; ensure compliance and inspection readiness; lead process improvement initiatives. Requirements: 6+ years in clinical site start-up and operations; experience with Phase 4, post-marketing, or real-world studies preferred; strong leadership, communication, and data-driven decision skills; familiarity with clinical trial systems such as CTMS (Veeva preferred). HighValue: late-phase studies, Phase 4, post-marketing, real-world data, clinical site management, metrics-driven improvements, CTMS systems. WorkSetup: full-time in the U.S., no visa sponsorship; collaborative, cross-functional environment.