Senior Director Trial Optimization and Feasibility

Role: Senior Director, Head of Trial Optimization & Feasibility, responsible for establishing and governing Teva’s global sponsor-side trial feasibility, enrollment forecasting, and protocol optimization models. Responsibilities: define evidence standards for CRO feasibility assessments, build internal analytics for enrollment prediction, validate and challenge CRO assumptions, develop country/site strategies, lead protocol operability reviews, and ensure continuous forecast accuracy improvement. Qualifications: 12+ years in global clinical development, with significant trial optimization and feasibility leadership; Bachelor's degree required; experience in complex, outsourced trial environments preferred. High-Value: focus on innovative portfolios, expertise in neuroscience and immunology advantageous, role involves cross-functional influence across R&D, Clinical Operations, Medical Affairs, and Analytics. Additional details include building sophisticated forecasting models, incorporating digital health, diversity, and sustainability considerations, and owning governance of feasibility processes. The role reports to senior leadership and influences enterprise standards. Work setup and travel specifics are not detailed.