About this role
CRA I - Guangzhou at Syneos - Commercial & Clinical/Corporation. Location: Guangzhou, Guangdong, China. Role: conducting monitoring, developing tools, managing projects Requirements: Bachelor's degree or equivalent,2-4 years clinical research monitoring experience,knowledge of GCP and regulatory requirements,proficiency with clinical trial management systems and Microsoft Office,CCRA preferred. Category: Research and Development (R&D) Seniority: Entry Level Tools: clinical trial management systems, Microsoft Office Certifications: ccra Commitment: Full Time Workplace: Hybrid Languages: English