Clinical research professional with over 15 years of experience in ophthalmology, including extensive involvement in retina-focused clinical trials. Skilled in patient recruitment, regulatory documentation, source data verification, and protocol compliance under GCP and FDA guidelines. Proven ability to collaborate with investigators and site staff, support sponsor monitoring visits, and maintain audit-ready documentation. Brings hands-on expertise in assisting with ophthalmic procedures, coordinating study operations, and ensuring data accuracy across multiple trials.