About this role
Clinical Research Associate/CRA I - FSP at Parexel. Location: United States or Tennessee or Pennsylvania. Role: managing sites, monitoring sites, ensuring compliance Requirements: Minimum 2 years direct site monitoring experience; strong site management, GCP/ICH knowledge, communication, data analysis, and IT skills; current driver’s license and ability to travel extensively. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Office, Clinical Trial Management System, electronic Trial Master File Certifications: driver Commitment: Full Time Workplace: Remote Languages: English