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
• Perform multiple imaging procedures required by study protocols

Requirements

• ICH GCP Training/Certification
• Certified Ophthalmic Assistant
• Ability to perform venipunctures and process samples with training
• Proficiency in Google, Microsoft Office, and Teams
• Ability to master ophthalmology and retina terminology
• Capacity to perform multiple imaging procedures and vision testing

Preferred Qualifications

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

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.