-
3-4年经验 -
本科 -
招若干人 -
11-20 发布
- 五险一金
- 补充医疗保险
- 补充公积金
- 员工旅游
- 交通补贴
- 通讯补贴
- 年终奖金
- 绩效奖金
- 定期体检
职位描述
职位描述： ？Performing management activities to clinical trial start up, budget control, initiation, patient enrollment, protocol adherence, CRF compliance, data quality so that they meet specified ethical, scientific, regulatory needs. Developing and maintain KOL relationships.？Maintains good communications and relationships with CRO partners, including but not limited to CRC, CRA, PM or DM if applicable.？Responsible for tracking, distribution and filing of clinical trial documents/information with quality review for accuracy and completeness.？Responsible for the clinical trial meets ICH – GCP guidelines, local regulatory requirements, protocol.？Supports and coordinates the clinical trial application for amendment and progress report to ethics committee and regulatory authority, if applicable, and obtain approval within required timeline.？Organizes appropriate training programs and project teleconferences as applicable.？Maintains / develops local tracking spreadsheets for study-related documents, data, tasks and activities, as applicable. 职能类别： 生物工程/生物制药
联系方式
爱迪生路275号
公司信息
华领医药技术（上海）有限公司是一家立足中国，面向全球，专注于全球领先创新药物研发和产业化的新型医药公司。公司目前的研发领域包括2型糖尿病治疗药物和中枢神经系统紊乱治疗药物 Hua Medicine is a leading clinical-stage, innovative drug development company in China, focusing on novel therapies for the treatment of diabetes and CNS disorders.
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