Clinical Research Coordinator

Job Description Seeking a Clinical Research Coordinator in San Marcos, TX Key Responsibilities Coordinate ophthalmic clinical trials (Phases I–IV) with a focus in retina. Serve as a lead coordinator across multiple studies, working as both masked and unmasked CRC. Manage EDC data entry, complete system-specific trainings, and resolve data queries. Recruit, screen, and retain study participants, including medical history documentation and review. Perform subject assessments including vitals, lab draws, and diagnostic testing. Maintain and organize regulatory documents in compliance with sponsor and CRO requirements. Collaborate with study sponsors, monitors, and CROs throughout the clinical trial lifecycle. Oversee investigational product (IP) management, including training, storage, temperature monitoring, shipping/receiving, dispensing/destruction, and accountability logs. Conduct IP inventory, reconciliation, and ensure protocol compliance for administration. Support site feasibility assessments, qualification visits, and study questionnaires. Partner with CRO teams on study submissions, continuing reviews, adverse event reporting, query resolution, and study close-out. Compensation Pay rate: $65-85K (Depending on experience) Schedule Schedule: Full time, onsite, 40 hrs a week #J-18808-Ljbffr