Associate Director, Clinical Development Trial Lead (CDTL)

Role: Lead complex, cross-functional clinical trials as Associate Director, Clinical Development Trial Lead (CDTL), with regional and global accountability for timely, quality delivery within scope and budget. Responsibilities: independently manage study teams, develop trial strategies, oversee project timelines, budgets, risks, and regulatory compliance; serve as CRO contact; influence study design; ensure inspection readiness; and mentor peers. Requirements: Bachelor's degree in a scientific or health-related field; 5+ years clinical research experience, preferably with oncology, early-phase trials, or radioligand therapy; strong project management skills; experience with global/regional trial processes; proficiency in project management tools; and ability to operate cross-culturally. Preferred: oncology expertise, radioligand therapy knowledge, leadership in process improvement, and experience with local/country regulatory requirements. High-Value: oncology, early-phase, cross-functional leadership, global/regional trial management, CRO oversight, inspection readiness, scientific and regulatory expertise. Work setup: onsite at Stamford, CT or Indianapolis, IN, with periodic travel.