Additionally, this role oversees subject enrollment tracking, monitors Case Report Form (CRF) data quality, and ensure all participant data, informed consent forms (ICFs), and Adverse Event (AE) reporting are accurate, legible, and fully compliant with ALCOA+ source documentation principles inside the Trial Master File (TMF). Manage day-to-day ophthalmic Rx program and device logistics and Collaborate with cross-functional partners including Clinical, Research Scientists, UX Researchers, Hardware/Software Engineering, and Regulatory to track program and study requirements, maintain schedules, and monitor study-readiness and compliance criteria.