About this role
CRA I - Guangzhou at Syneoshealth. Location: Guangzhou, Guangdong, China. Role: monitoring studies, writing reports, coordinating visits Requirements: 2+ years clinical research monitoring experience, GCP knowledge, bachelor's degree or equivalent, strong communication, and proficiency with clinical trial systems and Microsoft Office. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Office Suite Certifications: ccra Commitment: Full Time Workplace: Hybrid Languages: English