Description
The Associate Director, Clinical Development Trial Lead (CDTL) independently leads cross-functional study teams through the development, execution, and closure of complex local, regional, and global clinical trials. The role owns enrollment strategy, trial budgets, risk and issue management, TPO qualification, CRO oversight, inspection readiness, regulatory and scientific consultation, and regional operational processes. It requires a bachelor's degree, at least five years of clinical research or relevant scientific or health-related experience, and preferably onsite work in Stamford, Connecticut, or Indianapolis, Indiana, with remote options considered.
