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À̸ÞÀÏ: sonia.oh@docsglobal.com (or sunyoung.oh@iconplc.com)
Working proactively as part of a project team you will coordinate all necessary activities required to gain Regulatory & Ethics Committee approval for clinical studies.
You will be required to collate and prepare all documentation and dossiers for regional study approval in accordance with the relevant local legislations.
Regular contact with the designated personnel from Regulatory Authorities & Ethics Committees must be maintained in order to monitor the submission progress in accordance with study start up deadlines.
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