Associate Director, Clinical Development Trial Lead (CDTL)

Role: Lead cross-functional clinical trial teams as Associate Director, Clinical Development Trial Lead, overseeing complex global studies to ensure timely, quality delivery within scope and budget. Responsibilities: develop and manage trial plans, timelines, budgets, and risk assessments; lead study execution, vendor oversight, and regional enrollment strategies; ensure inspection readiness and track trial documentation; influence study design based on scientific and regional insights; and serve as CRO contact. Requirements: Bachelor's in a scientific/health-related field; 5+ years of clinical research experience, with strong project management skills; expert knowledge of GCP, trial processes, and regional regulatory requirements; experience in early-phase oncology, particularly radioligand therapy preferred. Preferred skills include cross-cultural collaboration, leadership, strategic adaptability, and proficiency with project tools (e.g., MS Project, PowerBI). HighValue: oncology, early-phase trials, radioligand therapy, global/regional trial management, CRO oversight. Work setup: onsite in Stamford, CT or Indianapolis, IN, with periodic travel.