Associate Director, Study Feasibility

Role: Study Feasibility Associate Director within AbbVie's Clinical Development Operations, focusing on global strategy and operational assessment for Phase 2 and 3 clinical trials. Responsibilities: facilitate cross-functional discussions with senior leaders to evaluate feasibility, support planning for large-scale studies across multiple countries, and optimize patient recruitment, site selection, and study timelines through scientific and operational analyses. Lead projects to enhance team capabilities and study performance, with an emphasis on strategic consultation across therapeutic areas such as Oncology, Neurology, or Immunology. Requirements: minimum 8 years in pharmaceutical or clinical research, with 5+ years in leadership roles; bachelor's or advanced degree in sciences; strong knowledge of drug development processes; proven expertise in complex scientific and operational decision-making. Preferred: therapeutic area background in Oncology, Neurology, or Immunology; experience in drug development or scientific project leadership. HighValue: oversight of global Phase 2/3 studies, multi-country operations, strategic planning, cross-functional leadership. WorkSetup: not specified; role involves collaboration with senior leaders across global sites.