About this role
Clinical Research Associate II - 苏州 at Parexel. Location: Shanghai or Suzhou or China. Role: managing sites, conducting visits, reviewing documentation Requirements: Site management experience in clinical research; ability to conduct on-site and remote monitoring, ensure compliance with ICH-GCP, maintain CTMS/TMF/EDC records, strong communication and problem-solving, willingness to travel and hold a driver’s license as required. Category: Research and Development (R&D) Seniority: Mid Level Tools: CTMS, EDC, IVRS, SIS, Electronic Document Management System (EDMS), Microsoft Excel, Microsoft Word Commitment: Full Time Workplace: Field Languages: English