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CRA II - Late Phase

Beijing
Permanent
Reference: JR061723_1571887148
Description

Role Responsibility

Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases IV ensuring that applicable regulations and principles of ICG-GCP are adhered to Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required Managing sponsor generated queries efficiently and responsible for study cost effectiveness Dependent on level of experience you may assist in training and mentoring less experienced CRA's and/or manage CRA's working on international projects

Experience and Qualification

Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data Native Chinese level and conversational English at least Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner Ability to produce accurate work to tight deadlines within a pressurized environment

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