■Maintaining organizational structure and documentation necessary for regulatory submissions of products related to clinical trials and post-market studies. ■Managing communication with regulatory authorities concerning clinical trials and post-market studies (including preparation for various consultations, creation and submission of documents, plans, reports, handling inquiries, and compliance investigations, etc.) ■Selecting and maintaining external contracting companies related to clinical trials and post-market studies. ■Drafting and managing budgets for clinical trials. ■Cooperating with overseas manufacturers to plan and coordinate tasks during the execution of clinical trials and post-market studies.
The above information is a public job ad. This job ad is neither an offer nor a contract.
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