About this role
Clinical Research Associate I/II at Parexel. Location: Chengdu, Sichuan, China. Role: managing sites, ensuring compliance, conducting visits Requirements: Site management and monitoring across study lifecycle, ensuring protocol and regulatory compliance, performing on-site and remote visits, updating CTMS/EDC/TMF, strong problem-solving and communication, ability to travel extensively and hold a driver’s license where required. Category: Research and Development (R&D) Seniority: Entry Level Tools: CTMS, EDC, IVRS, SIS, Electronic Document Management System (EDMS), Trial Master File (TMF), Microsoft Excel, Microsoft Word Commitment: Full Time Workplace: Remote Languages: English