Clinical Research Coordinator 257479

Medix™

Hattiesburg (MS)

On-site

USD 42,000 - 64,000

Full time

4 days ago
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Job summary

Medix is seeking a Clinical Research Coordinator in the United States to support trial activities in Hattiesburg, Mississippi. You will recruit subjects, coordinate visits and procedures, and ensure accurate data capture and regulatory compliance.

You will perform basic clinical measurements, handle specimens as required, and monitor participant safety while coordinating with the trial team and sponsor audits.

Responsibilities

  • Recruits, screens, and enrolls eligible study subjects with informed consent under PI guidance.
  • Coordinates and schedules participant visits, procedures, and study follow-ups from start-up to closeout.
  • Collects, records, and manages study data on source documents and EDC systems; resolves data queries promptly.
  • Prepares and maintains regulatory binders, IRB submissions, and essential trial documentation.
  • Performs basic clinical measurements (vitals, ECGs) and processes, stores, or ships biological specimens per protocol.
  • Monitors participant health, documents adverse events, and facilitates sponsor monitoring visits and audits.

Job description

  • Participant Management: Recruits, screens, and enrolls eligible study subjects; obtains informed consent under the guidance of the PI.
  • Study Coordination: Coordinates and schedules participant visits, clinical procedures, and follow-up care from start-up to study closeout.
  • Data & Documentation: Collects, records, and manages accurate study data on source documents and electronic data capture (EDC) systems; resolves data queries in a timely manner.
  • Regulatory Compliance: Prepares and maintains regulatory binders, IRB submissions, and essential trial documentation.
  • Clinical & Lab Duties: Performs basic clinical measurements (vitals, ECGs) and processes, stores, or ships biological lab specimens according to protocol.
  • Safety & Monitoring: Monitors participant health, captures adverse events, and facilitates sponsor monitoring visits and audits
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