Site Management Lead

Role: Senior/Lead Clinical Site Management (CSM) Lead supporting global clinical studies within AbbVie's development pipeline. Main objectives include ensuring the integrity, quality, and timely execution of site management activities across assigned studies. Responsibilities encompass driving study-level CSM deliverables, developing site monitoring and engagement strategies, overseeing monitoring activities, managing study risks, and ensuring inspection readiness. The role involves collaboration within the Clinical Study Team, influence across functional lines, and liaison with site monitors and country teams. Qualifications: Bachelor’s degree in a scientific or medical field; 5+ years in industry clinical research, with at least 2 years in monitoring or project management, preferably across multiple phases (I-III) and therapeutic areas. Experience in global, multi-phase clinical trials, including initiation through study completion, with knowledge of ICH, GxP, and regulatory compliance. Skills: strong leadership, communication, planning, and organizational abilities; proficiency in Microsoft Office tools; ability to influence without formal authority. High-value specifics: extensive experience in clinical trial site management, risk mitigation, and study compliance in a global setting. Work setup not specified but involvement in global, multi-site trials suggests a flexible or hybrid environment.