Clinical Research Coordinator: Participants & Study Ops

Medix™; Sacramento (CA); On-site; USD 55,000 - 95,000; Full time

Job summary

Medix is seeking a Clinical Study Coordinator in Sacramento, CA, to manage participant recruitment and consent under the PI, coordinate visits and procedures, and maintain trial data and regulatory documents. The role requires collaboration across clinical and lab activities to ensure protocol compliance.

Responsibilities include safety monitoring, adverse event reporting, and supporting sponsor visits and audits, with hands-on duties in vitals, ECGs, and specimen handling.

Responsibilities

• Recruits, screens, and enrolls eligible study subjects; obtains informed consent under the PI guidance.
• Coordinates and schedules participant visits, clinical procedures, and follow-up care 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 handles lab specimens per protocol.
• Monitors participant health, captures adverse events, and supports sponsor monitoring visits and audits.

Job description

Medix is seeking a Clinical Study Coordinator in Sacramento, CA, to manage participant recruitment and consent under the PI, coordinate visits and procedures, and maintain trial data and regulatory documents. The role requires collaboration across clinical and lab activities to ensure protocol compliance.

Responsibilities include safety monitoring, adverse event reporting, and supporting sponsor visits and audits, with hands-on duties in vitals, ECGs, and specimen handling.