Clinical Research Associate II/I

PSI CRO AG · Shanghai, China · full-time · On site · November 10, 2025

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Posted November 10, 2025 · Read from PSI CRO
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Job Description

As a Clinical Research Associate II/I at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

  • Conduct and report SSV, SIV, RMV, COV onsite monitoring visits
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions
  • Prepare and particiapte on audits and inspections

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • At least 2 years of independent on-site monitoring experience in China
  • Experience in all types of monitoring visits in Phase II and/or III
  • Therapeutic area experience in Oncology is a plus
  • Full working proficiency in English and Mandarin
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel, up to 70% of time

Additional Information

Advance your career in clinical research, overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated cross-functional teams, get all support and ownership of your projects.

  • Excellent working conditions
  • Extensive training and friendly, collegial team
  • Competitive salary package
  • Opportunities for personal and professional growth
Employer
PSI CRO AG
Location
Shanghai, China · On site
Contract
full-time