Responsibilities

The Manager II, Clinical Trials will oversee and manage key study activities such as study start-up, development of study plans, vendor management, drug inventory, lab supplies, and sample management, while also reviewing protocols, CRFs, and other study documents. They will participate in user acceptance testing, develop training materials and site study materials, assist in site qualification, ensure study staff are properly trained, arrange and oversee site visits, provide Sponsor oversight of monitoring activities, organize presentations, manage drug supply inventory, review study budgets, assist in creating project tools, review Clinical Study Reports, and serve as a resource for others within the company. Furthermore, the role involves developing study timelines, managing study finances and forecasting, and working cross-functionally to report on study status and strategy.