Associate Director, Study Feasibility

Role: Study Feasibility Associate Director within AbbVie's Clinical Development Operations, focusing on strategic assessment of global clinical trial feasibility and study design. Responsibilities: lead cross-functional discussions with senior leaders to evaluate operational aspects such as country/site selection, protocol review, patient burden, recruitment, and timelines; support planning for Phase 2 and 3 trials across multiple countries involving large study teams and substantial budgets; analyze scientific, operational, and strategic data to optimize study performance; provide guidance on country strategy and site selection; drive continuous improvement initiatives within the feasibility and recruitment teams. Requirements: minimum of 8 years in pharmaceutical/clinical research, with 5+ years in clinical project leadership; bachelor’s or advanced degree in sciences; strong understanding of pharma development processes; proven experience in complex scientific analysis and decision-making; leadership skills with strategic and scientific orientation. HighValue: experience in oncology, neurology, or immunology development; involvement in large-scale global Phase 2/3 trials; expertise in study design, operational feasibility, and cross-functional collaboration. WorkSetup: role involves global strategy and cross-functional engagement; specific location and travel details not provided.