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Associate Director, Regional Clinical Study Management

US · Remote · Full-time · Project Management

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About the role

GCPRisk Management
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Director, Regional Clinical Study Management based in the United States. This is a strategic clinical operations leadership role overseeing regional delivery of clinical studies and portfolios across the full study lifecycle. You will lead regional clinical operations teams and external partners while serving as a key escalation point for complex operational issues. The role combines strategic planning, study execution, quality oversight, resource management, and cross-functional leadership. You will help shape feasibility, country and site selection, recruitment, regulatory submissions, data collection, and study closeout activities. A strong focus on inspection readiness, ICH/GCP compliance, operational excellence, and risk management will be central to your impact. You will collaborate closely with global study teams, country leadership, vendors, medical affairs, regulatory teams, and senior management. This remote U.S.-based opportunity is suited to an experienced clinical operations leader who thrives in a fast-paced, international, and highly collaborative environment.