Description
The Clinical Research Coordinator oversees clinical research studies, coordinates with sponsors and CROs, prepares budgets and study materials, manages site readiness and regulatory documentation, supports subject recruitment and enrollment, conducts protocol-related testing and source documentation, and assists with adverse-event reporting and follow-up care. The role requires at least a high school diploma, CCRC or higher, at least one year of ophthalmic or optometric experience, knowledge of ocular anatomy and common conditions, and proficiency with spreadsheet and word-processing software. The work is performed in an office environment, may require travel to other CVP locations, and involves exposure to blood, bodily fluids, and cleaning supplies.
