Clinical Research Associate II/I

About the role

PSI seeks a Clinical Research Associate II/I based in Shanghai or Beijing to conduct and report onsite monitoring visits, perform CRF review, source document verification and query resolution, manage sites, support regulatory submissions, and prepare for audits and inspections. The role requires at least two years of independent onsite monitoring experience in China, Phase II and/or III monitoring experience, English and Mandarin proficiency, and travel up to 70%.

Key requirements

• • College/University degree in Life Sciences or an equivalent combination of education, training & experience
• • At least 2 years of relevant experience
• • Required skills: Independent on-site monitoring experience in China, Monitoring visits in Phase II and/or III clinical studies, SSV, SIV, RMV and COV onsite monitoring visits, CRF review, Source document verification, Query resolution, Site communication and management, Feasibility research, Regulatory document preparation, Audit and inspection preparation, MS Office applications, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel up to 70% of the time
• • Required languages: English, Mandarin

Opportunity details

• • Workplace: On Site
• • Posted: Nov 10, 2025
• • Original advert language: English

Full vacancy

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