CRA Intern in Shanghai: assist the CRA with basic source data verification at the study site per protocol, contract scope, SOP and GCP; assist with clinical trial documentation organization; perform other tasks as assigned by the line manager or PM. Requires a bachelor degree or higher (pharma-related preferred), CET-4 or above, and ability to intern at least 3 days per week for 3 months or longer.
Details
- Work type
- Onsite
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