CRA I
About the role
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- 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
- 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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Reasonable AccomodationsDay in the life
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