Clinical Research Associate I/II
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Job Description
Clinical Research Associate implementing and monitoring clinical trials for Parexel in China. Ensuring compliance with regulatory requirements and effective communication with investigative sites.
Responsibilities:
- Implement and monitor clinical trials
- Review and verify trial data accuracy
- Communicate with investigative sites
- Complete monitoring activity documents
- Facilitate audits and audit resolution
Requirements:
- 1+ years of clinical research experience
- Knowledge of ICH GCP guidelines
- Proficiency in monitoring and site management
- Ability to communicate effectively with investigators
- Must be fluent in English.
Benefits:
- Professional development opportunities
- Health insurance
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