Job Description

Job Summary

The Research Coordinator is responsible for coordinating research patient visits in compliance with ICH-GCP guidelines, IRB-approved protocols, and study manuals. This role involves ensuring study accuracy, regulatory compliance, and patient safety while collaborating with the study team to meet organizational goals.

Key Responsibilities

• Coordinate daily clinical trial activities, including scheduling and patient recruitment.
• Administer study questionnaires and manage inventory of study supplies.
• Train staff on protocols, informed consent, and study-specific procedures.
• Create and maintain source documents and data entries in EDC systems.
• Screen, enroll, and consent participants according to study protocols.
• Report adverse events (AEs/SAEs) and ensure compliance with reporting timelines.
• Monitor regulatory documentation, including IRB submissions and safety reports.
• Prepare for and assist with monitoring visits and audits.

Requirements:

• Bachelor's/Associate's degree or equivalent experience
• 2+ years of experience in Clinical Research
• Ophthalmology experience (preferred)

Details:

Location: Madison, MS

Pay: $25-$31/hr (Dependent on background and years of experience)

Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week

Duration: Contract to Hire (1040 Hours)

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