1 生命科學、醫療保健、製藥 職務 台灣
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Taipei, 台灣 Permanent
發佈於: 2024/10/4
Responsibilities: Design and develop protocols, informed consent forms, and case report forms. Write clinical study reports and brochures for clinical investigators. Draft Common Technical Documents for submissions, such as IND and NDA. Prepare integrated reports, annual updates, and speciali...