About this role
Clinical Research Associate II-武汉 at Parexel. Location: Chengdu or Wuhan or China. Role: monitoring trials, verifying data, mentoring staff Requirements: Implements and monitors clinical trials per ICH GCP; conducts site qualification and initiation; performs source document verification, data review, IP accountability, SAE verification, monitoring documentation, and mentors junior CRAs. Category: Research and Development (R&D) Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English