Clinical Research Coordinator 258919

Medix™; Sacramento (CA); Sur place; USD 55 000 - 95 000; Plein temps

Résumé du poste

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.

Responsabilités

• 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.

Description du poste

• 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