Azul Vision·Pasadena, California
The coordinator manages clinical research studies in the eyecare industry, overseeing patient recruitment, trial protocols, and regulatory compliance. They are responsible for data collection, performing ophthalmic tests, and coordinating with pharmaceutical sponsors and IRB.
A high school diploma is required, though a bachelor's degree is preferred, along with at least 2 years of clinical research experience. Prior experience as an ophthalmic technician and knowledge of eye anatomy is highly desired.
Market context
Clinical Research Coordinator jobs in California are often tied to hospitals, academic medical centers, and research sites that need careful study coordination and patient-facing communication. This role is competitive because employers look for strong interpersonal skills, attention to detail, and the ability to keep pace in a busy clinical setting; the requirements and benefits on this platform are AI-summarized from the original job description, saving you research time. Before applying, review your experience with study documentation, participant coordination, and fast-paced clinical workflows.