Demo

Clinical Research Coordinator

Medix
Flowood, MS Full Time
POSTED ON 3/3/2025
AVAILABLE BEFORE 6/3/2025

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)

    Salary : $25 - $31

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