• Responsible for providing general administrative and project tracking support, as well as assisting the clinical research teams in study conduct.• Set-up, organize, maintain and archive clinical study documentation (electronic and/ or paper-based)• Assist project teams with study-specific documentation and guidelines • Assist with review of study documents for accuracy and completeness • Under direction of management create and maintain internal documents• Manage… Show more • Responsible for providing general administrative and project tracking support, as well as assisting the clinical research teams in study conduct.• Set-up, organize, maintain and archive clinical study documentation (electronic and/ or paper-based)• Assist project teams with study-specific documentation and guidelines • Assist with review of study documents for accuracy and completeness • Under direction of management create and maintain internal documents• Manage documentation to ensure high levels of accuracy• Assist with tracking and management of Case Report Forms (CRF), queries, and clinical data flow• Log and track project progress, incoming/ outgoing documentation and correspondence, and associate documentation• Assist with quality control audits of internal and clinical study documentation• Fulfill any other duties as required Show less

了解药企组成，运行，日常工作。 学习药品注册规范，简单药品注册工作，资料整理工作。 专业培训，学习。