岗位职责:
1.在上级的指导下协助制定实验方案；
Assisting designing study plan under the guidance of superior;
2.负责参与新药的药代动力学试验的具体实施、生物样品分析，数据整理和报告撰写；
Responsible for participating in conducting PK experiments, biological sample analysis, data sorting and report writing;
3.配合相关人员完成实验报告撰写及药品注册申报资料准备；
Assisting writing study reports and the IND/NDA application documents;
4.负责参与临床前制剂筛选和体系搭建；
Responsible for participating in preclinical formulation screening and platform development;
5.完成上级安排的其他任务。
Assisting your superior with other tasks.
任职要求:
1.硕士，药代动力学、生物样品分析或相关专业，1年以上工作经验；
MS in pharmacokinetics or related disciplines with 1+ year training/working experience;
2.熟练掌握LC/MS/MS等仪器、WinNonlin软件的使用；
Good command of LC/MS/MS instruments and WinNonlin software;
3.具有良好的查阅及总结国外文献的能力；
Good skills in searching and collecting information;
4.具有优良的团队协作精神，工作积极主动、创新精神。
Good collaboration, motivation and innovation;
5.熟练使用PPT、Word、Excel、Prism等工作软件。
Good practice in the use of PPT, Word, Excel and Prism softwares.