Responsibilities Support clinical development planning and execution to align with customer’s clinical trial project request and quality standard. By interacting with various key functions (for example clinical operation, biometrics, quality assurance and pharmacovigilance), this position will provide clinical expertise to conduct and manage project related medical monitoring. He/she shall deliver high quality clinical scientific services by providing medical input to protocol, contributing to protocol adaptation, conducting medical writing, and relevant activities. He / she shall also build and maintain good medical science relationships internally with all functional lines within the company and externally with KOLs and investigators. He / she will have the exposure to different project teams, diverse portfolio of clients, as well as various therapeutic areas. Requirements 1.Master degree or other life science degrees (or equivalent); clinic practice is required 2.Minimum 2 years of experience as physician or medical manager in biopharmaceutical industry 3.Experiences in medical monitoring 4.Experiences in providing medical and scientific advices on clinical trial protocol design and other clinical development strategies 备注： ‘职位年薪’ 仅供参考，具体薪资和福利将根据候选人经验和能力综合评定。