About this role
Clinical Research Associate at Alirahealth. Location: Boston or United States or North America. Role: monitoring sites, reviewing reports, ensuring compliance Requirements: Experienced CRA to perform site monitoring, ensure protocol/GCP compliance, prepare monitoring reports, manage study documentation, and support site training and issue resolution; ability to travel and work across time zones. Category: Research and Development (R&D) Seniority: Mid Level Tools: Clinical Trial Management System (CTMS), eTMF/TMF, electronic data capture Certifications: certified monitor Commitment: Full Time Workplace: Remote Languages: English