Clinical Research Coordinator - 227662 Job at Medix™, Meridian, MS

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  • Medix™
  • Meridian, MS

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)

Job Tags

Contract work, Monday to Friday,

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