Associate Director, Study Feasibility

Role: Study Feasibility Associate Director within AbbVie's Clinical Development Operations, focusing on strategic planning and operational feasibility for global Phase 2 and 3 trials. Responsibilities: lead cross-functional discussions with senior leaders on site/country selection, protocol review, patient burden, recruitment, and timelines; support large-scale studies across 35+ countries with budgets over $200 million; perform detailed scientific and operational analyses; provide strategic consultation and optimize study performance across therapeutic areas like Oncology, Neurology, or Immunology; lead initiatives to enhance team capabilities. Requirements: minimum 8 years of pharma experience, with at least 5 in clinical research or project leadership; bachelor’s or advanced degree in sciences; strong knowledge of drug development processes; recognized analytical and scientific decision-making skills; leadership experience; therapeutic background preferred. HighValue: global Phase 2/3 trials, multi-country studies, therapeutic areas (Oncology/Neurology/Immunology), cross-functional leadership, scientific and operational expertise, large budgets, and strategic planning.