Travel Clinical Research Coordinator

Job Summary

To support a growing clinical research team, the full-time Travel Clinical Research Coordinator will manage patient screening, consent processes, and follow-up visits while ensuring compliance with study protocols and regulatory guidelines in a fully remote environment.

Key Responsibilities

• Screen patients for study enrollment and conduct follow-up visits while documenting in source clinic charts
• Manage data entry in electronic data capture systems and maintain study-specific logs and supplies
• Coordinate with the Site Manager/Director and Principal/Sub Investigators to ensure compliance with FDA, GCP, and ICH regulations

Required Qualifications

• A Medical Assistant diploma, LPN/LVN, EMT credential, or equivalent combination of education and experience with 2+ years of clinical research coordination experience
• Experience with basic clinical procedures such as blood pressure, vitals, EKGs, and phlebotomy
• Vaccine trial experience is required
• Proficiency in Microsoft applications and electronic health records
• Bi-lingual proficiency in English and Spanish is a plus