- 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 2-3 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
- Excellent working conditions
- Extensive training and friendly, collegial team
- Competitive salary package
- Opportunities for personal and professional growth
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Clinical Research Associate II - Shanghai, 中国 - PSI
描述
Job Description
As a Clinical Research Associate II 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:
Qualifications
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.
