Clinical Research Associate II
4 weeks ago
Job Overview
As a Clinical Research Associate II at PSI, you will be responsible for conducting and reporting onsite monitoring visits, performing CRF review and source document verification, and managing site communication and support services.
Key Responsibilities
- Conduct and report SSV, SIV, RMV, and COV onsite monitoring visits
- Perform CRF review and source document verification
- Manage site communication and support services
- 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 participate in audits and inspections
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training, and experience
- At least 2-3 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
What We Offer
- Excellent working conditions
- Extensive training and friendly, collegial team
- Competitive salary package
- Opportunities for personal and professional growth
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