Actualizado a 27 Março 2019
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Girija Gadikopala

Resumo

 Supervise collection of ongoing study data for the purpose of regular project status reporting  Review study related documentation for compliance with SOP and ICH GCP guidelines - Ensure Adverse Events are reported appropriately, accurately and in a timely manner and that follow-up activities are conducted as necessary.  Assist the General manager, clinical operation managers with the

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