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Clinical Research Associate

Fa Euzi Saasfaprod1 · Taiwan

Clinical TrialsJunior LevelExternal listingfull-time22 days ago

About The Role

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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