Mylene Mandret is a Global Project Manager with nearly 20 years of clinical research experience, including more than eight years leading global clinical trials and cross-functional project teams. Her experience spans Phase I–III drug development, with a strong focus on oncology and complex early-phase programs. She has led first-in human studies, study start-up, dose escalation activities, risk management, vendor oversight, and global study delivery. Her work focuses on coordinating critical study dependencies, strengthening cross-functional execution, and helping teams translate complex operational challenges into clear, actionable plans that support timely clinical development decisions.