Global Trial Lead (multiple openings)

Role: Serve as Global Trial Lead, owning end-to-end operational oversight of global medical studies across all phases, ensuring timely, within-budget, and compliant execution. Responsibilities: manage study delivery, vendor relationships, risk mitigation, and study-level planning; collaborate with the MEG Lead on protocol and medical oversight; oversee budgets, resource planning, vendor scope, and quality standards; ensure regulatory compliance and data integrity through systems like Veeva; lead global initiatives and represent operational execution in governance forums. Requirements: BA/BS in a relevant discipline; minimum 4 years in clinical/medical operations and project management within pharma or healthcare; experience leading global clinical trials, managing CROs, and cross-functional teams; knowledge of clinical trial phases, therapeutic areas, GxP, and systems such as CTMS; able to work across multiple geographies with up to 25% travel. Preferred: multi-national experience, vendor management expertise. High-Value: global clinical trial management, operational accountability from start-up through close-out, strong vendor and risk management, regulatory compliance, and cross-functional collaboration in the biopharma setting.