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临床医学/Clinical Research Physician

缔脉生物医药科技(上海)有限公司

浦东新区-张江镇 | 3-4年工作经验 | 硕士

2020-10-17发布

招聘人数:2人

100000-300000元/年

申请职位

职位信息

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。

联系方式

上班地址:上海市浦东新区祥科路298号佑越国际3楼301-305

缔脉生物医药科技(上海)有限公司


?民营公司

? 少于50人

? 制药/生物工程

缔脉生物医药科技(上海)有限公司是一家临床合同研究组织(CRO),旨在为中国及全球生物医药公司和医疗器械公司提供高水准全方位的服务,以我们专业能力、全球经验、先进技术和创新方法确保临床试验符合科学规范和满足法规和监管要求。我们希望推动国内临床开发水平和技能的不断提升从而促进中国创新药物走向全球,同时我们也希望以创新致力于提高临床试验的规划和执行效率,从而最终增大客户药物和医疗器械的成功几率。缔脉聚集了大批具有国际视野的、在临床试验方面具有丰富经验的专业人才,我们的主营业务包括专家咨询、临床试验运营、生物统计与编程、数据管理、药物安全与警戒、临床科学与医学事务、质量保证、稽查及核查准备、法规事务和策略等。
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