Round Rock -Clinical Research Coordinator I
On-site · Round Rock, Texas, United States
Job Summary
Clinical Research Coordinator I in a retina practice responsible for coordinating daily clinical trial activities, ensuring adherence to GCP/IATA standards, creating and maintaining study source documents, overseeing IRB and regulatory requirements, and coordinating communication with study sponsors, monitors, and CROs. Duties include attending teleconferences, training staff on study protocols, performing imaging and vision testing, screening patients for eligibility, obtaining informed consent, managing data entry in EDC systems, and supporting patient care during visits while safeguarding protocol confidentiality and timelines.
Required Qualifications
- Certified Ophthalmic Assistant
- ICH GCP Training/Certification
- Master multiple computer systems including Google, MicrosoftOffice, Teams
- Ability to develop and maintain strong relationships with physicians, coworkers, and patients
- Ability to perform venipunctures and process samples with training provided
- Train and certify to perform refraction and vision testing
Desired Qualifications
- CRA tier III and/or 18 months with prior performance review or assessment exceeding expectations
- Bilingual in Spanish
- Ophthalmic imaging on OIS/Topcon, Heidelberg and Optos
- FA, FP, FAF, and IR imaging on Heidelberg and Cirrus systems
- CCRP or CCRC Certification
- Real Time CTMS experience
- Experience with ophthalmology or retina terminology
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