-Act as contact for project team and study sties
-perform CRF review, query generation and resolution under supervision of Covance or client data management system.
-Assist in communication with sites to resolve the issues and data
-Assist with study supply management
-Create, update and track study trial tracker, tools, systems.
-Assist local project team with other admin work as required.
-Ensure compliance with Covance SOP, ICH GCP
university/college degree with life science preferred.
-1 or more year experience of relevant clinical research field in phar or CRO
- basic understandig of biology and process
- good organization and time managment skills
- good communcation and computer skill
- work efficiently
- fluent in local language and English
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