Clinical Trial Coordinator: Patient-Centric Research Ops

Medix™; Hattiesburg (MS); On-site; USD 42,000 - 64,000; Full time

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

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.