Senior Director, Head of US Site Management

Role: Senior Director, Head of US Site Management, overseeing all US site-facing clinical trial activities across Bayer’s development portfolio. Core responsibilities include leading US site management, study start-up, monitoring, enrollment optimization, and execution strategies; developing scalable, risk-based monitoring models; forging strategic site partnerships; and ensuring compliance with ICH-GCP and regulatory standards. The role also involves vendor oversight, process improvement through digital innovation, and maintaining inspection readiness. Collaborates closely with cross-functional teams such as Clinical Development, Data Management, Quality, Regulatory, and Medical Affairs, reporting to senior leadership. The position entails building high-performing teams, managing up to 50% travel domestically and internationally, and supporting strategic initiatives. Qualifications include a Bachelor's in life sciences or healthcare, 12+ years (or 10+ with an advanced degree) in clinical operations, strong US trial start-up, site management, and monitoring expertise, with knowledge of regulatory compliance, vendor management, and inspection processes. Preferred candidates have advanced degrees (PhD, MBA) and experience supporting regulatory inspections and implementing innovative digital tools. High-value biopharma specifics involve clinical trials in complex development stages, emphasizing operational leadership, risk management, and strategic partnership development within a global pharmaceutical setting.