What are the responsibilities and job description for the Clinical Research Coordinator position at Medix?
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 :
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
