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Clinical Research Associate Hunan

ShanghaiPosted 3 months ago
Full-timemid

Job Description

CRAs Contribute comments/input in the development of Protocol, Informed Consent Form (ICF), Case Report Forms (CRF) and other project related documents. Evaluation potential sites with the assistance from the senior CRA, PM or line manager and provide PM with recommendations for selection of qualified sites.

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Clinical Research Associate Hunan at Novotech | Renata