岗位职责:
1.负责组建，领导和培训细胞治疗板块，协调CRO、医院及各类研究机构的项目合作;
2.主导公司细胞治疗项目的调研、立项，参与制定公司研发的发展战略和产品研究方向敏锐发现有潜力的细胞治疗产品;
3.负责细胞治疗项目的靶点发现、靶点验证、作用机制研究、平台构建，协助 IIT 临床;
4.解决临床前开发阶段可能遇到的生物学、毒理及 CMC 等相关问题;协助 IND 申报和临床开发策略;
5.定期主持团队内部会议，通报项目进展及存在问题，并向上级领导汇报;
6.定期收集国内外细胞治疗的前沿研究，协助研发中心完成商务拓展时的相关尽调工作;
7.建立和维持关键专家、学科领域关键人物的关系，并保持与公司的研发目标相一致;


任职要求:
1.获得生物学、医学等相关领域的博士学位;
2.具有扎实的肿瘤免疫、自身免疫等相关背景，细胞治疗经验优先;
3.良好的中文和英文基础,具有优秀的领导能力、良好的团队合作精神和内外部沟通能力;
4.5 年以上创新药企业工作经验，且具备至少3年以上的团队管理经验。5.作为项目负责人，成功推进至少 1-2 个细胞治疗产品进入临床阶段;
6.熟悉 NMPA 和 FDA 药品注册法规及研发流程，具有较强的实验设计和分析能力，并能够对实验数据进行分析、归纳、整理和解读;

Responsibilities:
1. Responsible for building, managing, and training the cell therapy division.coordinating project collaborations with CROs, hospitals, and research institutions.
2. Spearhead the research, evaluation, and initiation of company cell therapy projects, participate in formulating R&D strategies and product development directions, and identify promising cell therapy products.
3. Oversee target discovery, validation, mechanism of action studies, and platform development for cell therapy projects, supporting llT clinical trials.
4. Address potential challenges in preclinical development, including biology, toxicology, and CMC-related issues; assist in lND submissions and clinical development strategies.
5.Regularly lead internal team meetings to communicate project progress and issues, reporting to senior management.
6. Stay updated on global advancements in cell therapy and support business development due diligence for the R&D center.
7. Establish and maintain relationships with key opinion leaders and industry experts, aligning with company R&D objectives.

Requirements:
1. Ph.D in biology, medicine, or related fields.
2. Strong background in tumor immunology, autoimmunity, etc.; cell
therapy experiences preferred.
3. Proficiency in Chinese and English, excellent leadership, teamwork, and communication skills.
4. 5+ years of experience in innovative drug development, including at least 3 years in team management.
5. As a project lead, successfully advanced 1-2 cell therapy products into clinical stages.
6. Familiarity with NMPA and FDA regulatory requirements and R&D processes, strong experimental design and analytical skills, with the ability to interpret and summarize data