Clinical Research Associate II/I

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

• 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

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