• Act as medical monitor in clinical ophthalmology studies with a focus on safety, data review and analysis of emerging data • Contribute to study related documents including but not limited to study synopsis, protocols, amendments, ICFs, IBs, INDs, annual reports, CSRs, and other regulatory submissions and project-related documents. Accountable for the medical content of documents. • Analyze, interpret, and organize data for presentations and publications • Interact with external experts to gather input. Organize scientific advisory board meetings and data safety monitoring committee meetings • Maintain a high level of clinical and scientific expertise in ophthalmologic disease area(s) by reviewing the literature and attending medical/scientific meetings • Ability to communicate with Investigators and research site staff to ensure rigorous and compliant study conduct • Able and willing to travel