月薪60000元 台北市信義區 3年工作經驗 4天前更新
General Description:
Develop clinical trial related documents for submission to regulatory authorities and/or IRB.
Clinical documents, including but not limited to:
1. Clinical study protocols and amendments,
2. Investigator brochures,
3. Clinical study reports,
4. Regulatory briefing documents,
5. Informed consent form
6. Clinical sections of INDs, NDAs, and
7. Other regulatory/IRB submission documents.
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