Site Management Lead

Role: Senior Manager or Lead for Clinical Site Management (CSM) within AbbVie's Clinical Development Operations, responsible for ensuring quality, integrity, and timely execution of site activities across studies. Key objectives include study-level planning, resource allocation, site selection, activation, engagement, monitoring, risk mitigation, and study close-out in collaboration with global teams. Responsibilities encompass leading CSM deliverables, overseeing monitoring activities, managing timelines, ensuring compliance with GxP, ICH, and regulatory standards, and maintaining inspection readiness. Qualifications: Bachelor's degree in a medical/scientific field, minimum 5+ years of industry clinical research experience, with at least 2 years in monitoring or project management on global studies. Experience spanning multiple phases (I-III) and therapeutic areas, with strong leadership, communication, and organizational skills. Proficiency in clinical trial processes, standards, and Microsoft Office tools. Preferred: exposure to multiple therapeutic areas, phases, or indications; demonstrated leadership in matrix environments; fluency in English. High-value: Experience in global multicenter studies, site management, risk assessment, and study lifecycle management; focus on compliance and quality assurance. Work setup: Not specified; typically involves cross-functional collaboration in a fast-paced environment.