主要职责：
1、调研整理产品相关的临床药理学及临床试验信息，参与制定产品临床药理学研发计划；
2、撰写临床药理学相关试验资料(方案，CSR等）；
3、分析处理临床药理试验中产生的数据；
4、协调准备临床研究中心立项伦理资料；
5、完成临床试验登记备案相关工作；
6、参与临床药理试验的实施推进工作。
任职资格
教育背景：临床药理相关专业，博士及以上
相关经验：无
语言要求：良好的中英文阅读、交流、写作能力
其他技能：熟练使用办公软件、良好的文献检索能力
能力要求
1. 具有较强的执行力；
2. 具有较强的独立科研能力及逻辑思维能力；
3. 具有清晰的书面和口头表达能力；
4. 具有较强的集体意识和良好的团队合作精神；
5. 具有良好的适应能力，能在时间限制和任务压力下工作；
6. 具有良好的职业道德。
Key Responsibilities:
Qualifications:
Education:
PhD or higher in Clinical Pharmacology or related field
Language Requirements:
Proficient in reading, communication, and writing in both Chinese and English
Other Skills: Proficient with office software
Competency Requirements:
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