• 无工作经验
  • 招若干人
  • 11-09 发布

职位描述

职位描述: 主要职责:1、参与研究基地及合作机构的评估筛选等前期准备工作;2、协助项目经理签署与研究中心协议;3、负责研究中心的伦理递交、分中心启动、研究中心培训、研究中心关闭等工作;4、负责项目监查,保证试验的实施符合GCP/ICH-GCP及SOPs,并协调解决在临床试验中发生的各种问题;5、协调试验用药的运输及处理,及时提供试验用药及其他试验相关的物资;6、协助方案、知情同意书及病例报告表及其它相关文件的撰写,并做好备案等工作;7、及时向项目经理沟通项目进展及相关的信息,并协助项目经理控制试验预算;8、指导和辅助初级监查员;9、参加团队会议,协同监查,执行其他与工作相关的职责分配。职位要求:1、临床医学、药学等医学相关专业,本科或以上学历;2、两年以上临床试验或相关领域的工作经验,理解ICH-GCP指导原则及法规;3、能适应出差,具有良好的沟通能力和较好的客户服务意识;4、有较强的独立工作能力及团队合作精神;5、优先考虑和管理多个任务的能力;6、善于阅读文献及资料撰写。7、具备英文沟通能力。 职能类别: 临床研究员

联系方式

上地三街嘉华大厦

公司信息

本公司为外商独资企业,总部位于美国马里兰州,是一家全球性医药研发咨询服务机构(CRO)。为满足业务发展需求,公司在全国各地广泛招聘各方面人才,包括临床监查、商务拓展、注册等职位,欢迎有才、有志者加盟。在北京,公司位于海淀区上地,工作地域优越、交通便利。 本公司发展以人为本。对优秀人才,公司提供: 优厚的工资、福利待遇(与跨国制药企业相当) 极大的个人发展空间与职务提升的潜力 多方面培训机会(包括去美国总部培训的安排) 和谐愉快的工作环境与团结协作的团队精神 本公司处于快速发展阶段,要求员工具备以下优良素质: 事业心强、富有敬业精神 有独立工作的能力与自我开拓精神 善于沟通 能吃苦耐劳 公司对有跨国公司经验的申请者优先考虑,有意者请发简历到所述邮箱并注明城市和所申请职位。 有符合所述条件者请发简历到本公司,否则不予考虑。一经录用,待遇优厚。 Accelovnace (China) Co. Limited is an international pharmaceutical service company. It is a CRO/SMO (a clinical research organization and site management organization). It is focused on global clinical trial management for western pharmaceutical and biotechnology industry; as supplementary, it also provides service to local pharmaceutical companies for clinical trial management. The Company is registered in Beijing as a wholly foreign owned enterprise. Its parents company is headquartered in Rockville, Maryland of the USA. Currently, the Company has 12 wholly self owned clinical sites throughout the United States. It is starting up its China operation in Beijing from June. 2005. As a US originated CRO/SMO, Accelovance always pursues the best clinical practice in clinical trial management, pursues quality, speed and cost-effective for its clients; demonstrate its professionals to its clients and investigators from details. With advanced patient and project management system, with electronic trial management system and web-based data capture system, with experienced and dedicated employees and systemic training and strong support from its parent company in the US, Accelovance (China) is able to deliver phase I to phase IV clinical trial operations for all kinds of clients. In the same time, Accelovance pays attention to personal advancement for its staff from competitive salary and benefit to long-term professional development opportunity, from systemic training to team building and open-minded culture. Accelovance is confident to abstract elites in clinical research industry. For more details, please visit the Company's website at www.accelovance.com.cn Notice: Applicants must fit for requirements, if not, please do not send your CV to us, thanks! 具有新药临床试验经验者优先录用

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