Evaluates prospective and awarded studies requiring CRU scheduling or placement assessment, partnering with the Feasibility Lead and relevant functional stakeholders to develop scheduling plans based on protocol requirements, participant and cohort needs, bed capacity, recruitment capability, procedural workload, specialized equipment and processing limitations, holidays, sponsor timelines, and competing site activity. Partners cross-functionally with Site Leadership, Site Investigators, Business Development, Participant Recruitment, Finance, and clinical operations teams to develop scheduling solutions, support business opportunities, and facilitate executable study placement and scheduling across individual and multisite studies.