Clinical Research Coordinator

About the role

This role allows you to leverage your existing hands-on ophthalmic expertise—such as patient prep, visual acuity testing, and clinic workflows—while gaining high-demand experience managing data and protocols for cutting-edge clinical trials.

Responsibilities

• Manage data collection and process data queries, ensuring resolution.
• Identify adverse events and reports per protocol guidelines.
• Assist in the planning and design of source documents for study protocols as required.
• Update and review regulatory documents, including annual IRB approvals, protocol amendments, and safety reports.
• Responsible for the timely completion of identified study documents, including case report forms.
• Ensure compliance with FDA and GCP guidelines.
• Conduct pre-study, initiation, monitoring, and close-out visits with sponsor representatives.

Qualifications

• High school diploma (or GED).
• One year of experience as a Clinical Research Assistant in an ophthalmic practice required.
• Retinal practice experience preferred.
• Training in medical terminology required.

Skills

• Site Initiation
• Patient Scheduling and Visit Coordination

Location: Dallas, Texas

Job type: Permanent

Salary: $52,000 – $58,000 per year

Work hours: 9 to 5