To be responsible for validation and implementation of quantitative bioanalytical assays in support of pre-clinical and clinical studies; GLP compliance experience is a plus.
Responsibilities:
1. Design, develop, and validate the immunoassays.
2. Analyze large molecule samples from pre-clinical or clinical studies using immunoassays.
3. Draft study reports, including assay development, validation, sample analysis reports; communicate with the Study Director or Principal Investigator
4. Responsible for instrument maintenance, including calibration and routine cleanups following laboratory SOPs.
5. Conduct projects and deliver the projects within proposed timeline; perform job assignment with minimal supervision from the management.
Requirement:
1. MS with biology, biochemistry or pharmacology background. Have experience in ELISA at least 2 years.
2. Hands-on experience on immunoassay implementation, validation, and sample analysis in a GLP work environment is a plus
3. Experience with immunogenicity assays is a significant plus.
4. Ability to reading, writing, speaking and understanding English.
负责临床前和临床研究的生物样本的验证和定量生物分析实验，有GLP经验者优先
岗位职责：
1. 独立完成方法的设计、开发、和验证工作；
2. 用免疫学方法分析临床前和临床研究的大分子样本；
3. 撰写研究报告，包括实验开发、验证、样本分析报告，并与总监和PI沟通研究结果；
4. 负责仪器的维护、校验等工作，日常整理实验室SOP等；
5. 按制定的时间节点，进行项目的分配，并按时完成项目工作。
任职要求：
1. 生物、生物化学、制药相关专业背景，硕士以上学历，至少2年ELISA相关实验的工作经验
2. 能独立完成免疫测定、验证和样本分析，熟悉GLP工作环境者优先
3. 有免疫学相关实验经验者优先
4. 优秀的英语听说读写能力
