Clinical Research Coordinator I

Responsibilities

• Facilitate and coordinate daily clinical trial activities and serve as primary coordinator for single-site studies
• Create, manage, and maintain source documents and regulatory information including IRB documents and investigator brochures
• Screen patients for eligibility using protocol-specific inclusion and exclusion criteria
• Provide patient care during visits, including diagnostic testing and patient education regarding study protocols
• Perform data entry in multiple Electronic Data Capture (EDC) systems
• Coordinate with study sponsors, monitors, and CROs regarding data queries, audits, and monitoring visits
• Collect and report medical history and adverse events to sponsors and the IRB

Requirements

• ICH GCP Training/Certification
• Certified Ophthalmic Assistant
• Ability to perform venipunctures and process samples
• Proficiency with Google Workspace, Microsoft Office, and Teams
• Ability to perform multiple imaging procedures and vision testing
• Strong relationship management skills with physicians and patients

Preferred Qualifications

• Bilingual in Spanish
• Ophthalmic experience
• College degree
• CCRP or CCRC Certification
• Experience with Real Time CTMS
• Experience with FA, FP, FAF, and IR imaging on OIS/Topcon, Heidelberg, and Optos
• Experience with SD-OCT scanning on Heidelberg and Cirrus systems

About the Company

Austin Retina Associates aims to advance retinal research, offer new treatment opportunities to the community, and provide the highest quality patient care.