工作职责：

工作职责：
1、负责临床前代谢方向（肥胖、糖尿病、NASH等）药效项目的全流程管理，把控实验进度、数据质量与交付节点。
2、主导试验方案（Protocol）设计及最终报告（Report）撰写，评估模型可行性及项目风险。
3、指导实验员完成模型构建与表型检测（GTT/ITT、代谢笼、生化/病理终点等），解决项目中的关键技术问题。
4、作为项目技术接口人，独立对接客户方案沟通与答疑，提供研发策略建议。

Responsibilities:
1.Lead full-process management of in vivo metabolic pharmacology programs (obesity, diabetes, NASH), with accountability for experimental progress, data integrity, and on-time delivery.
2.Lead protocol design and final report writing; evaluate model feasibility and project risks.
3.Supervise technical staff in model induction and phenotypic assessments (IPGTT/IPITT, metabolic cages, biochemical/histopathological endpoints), troubleshooting critical technical issues on the bench.
4.Act as the scientific point of contact for clients, independently driving protocol discussions, Q&A, and providing R&D strategy recommendations.

任职资格：

任职要求：
1、博士学历，生物、药学等相关专业，有肥胖、糖尿病、非酒精脂肪肝等代谢类疾病模型开发经验优先。
2、熟悉大小鼠动物实验操作，熟悉各类生化检测。
3、英语听说读写流畅，可以作为工作语言。
4、严谨细致，执行力强，具备良好的客户沟通能力、抗压能力与团队合作精神。

Requirements:
1.Ph.D. in Biological Sciences, Pharmacy, or related fields; hands-on experience in developing metabolic disease models (obesity, diabetes, NAFLD/NASH) preferred.
2.Proficient in mouse/rat surgical and experimental procedures; experienced in various biochemical assays.
3.Fluent in English (reading, writing, speaking, and listening); English as a working language.
4.Detail-oriented, execution-focused, with strong client communication skills, resilience, and team spirit.