Teams at Houston Retina Associates

Assists with clinical research patient visits under ICH-GCP and IRB-approved protocols. Coordinates subject appointments, prepares documentation, obtains consent, collects and records clinical data, transcribes information into electronic case report forms, administers questionnaires, performs ECGs and ophthalmic testing, processes biological samples, supports adverse event reporting, and helps resolve data queries.

Supports ophthalmic clinical research visits under ICH-GCP and IRB-approved protocols. Coordinates subject visits, prepares documentation, obtains consent, collects and enters study data, administers questionnaires, performs ECGs and vision testing, processes biological samples, scribes ocular exams, assists with patient care, and resolves data queries. Requires a bachelor’s degree or four years of ophthalmic experience in lieu of a degree; no prior experience is required for degree holders.

Assists with ophthalmology clinical research visits under ICH-GCP and IRB-approved protocols. Responsibilities include preparing patients, supporting treatments, collecting and recording study data, monitoring adverse events, performing intraocular pressure checks and post-treatment vision assessments, collecting aqueous humor samples, maintaining sterile instruments, calibrating equipment, stocking treatment rooms, and completing required training and documentation.