About this role
Insourced Clinical Research Associate at Caidya Group of Companies. Location: Beijing, Beijing, China. Role: monitoring sites, verifying documentation, reporting findings Requirements: 3+ years on-site clinical monitoring experience, college degree or 3+ years CRA experience, strong GCP/ICH knowledge, Microsoft Office skills, valid driver’s license and passport, strong communication and documentation skills. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Office Certifications: driver, passport Commitment: Full Time Workplace: Field Languages: English, Chinese