Job Description

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:

1. Research and compile product-related clinical pharmacology and clinical trial information; participate in developing clinical pharmacology R&D plans;
2. Draft clinical pharmacology-related trial documents (e.g., protocols, CSRs);
3. Analyse and process data generated from clinical pharmacology trials;
4. Coordinate and prepare materials for clinical research site initiation and ethics approval;
5. Complete clinical trial registration and filing-related tasks;
6. Participate in the implementation and advancement of clinical pharmacology trials.

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:

1. Strong execution ability
2. Strong independent research and logical thinking skills
3. Clear written and oral communication skills
4. Strong team spirit and good collaboration skills，good literature search ability
5. Good adaptability, able to work under time constraints and pressure
6. Strong professional ethics

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