clinical trial assistant (全职)
6K+元/月
  • 上海
  • 1 人
  • 1年及以上工作经验
  • 本科及以上
  • 五险一金
  • 晋升空间大
  • 带薪年假
  • 弹性工作制
  • 办公环境好
  • 员工旅游
  • 接受应届生
  • 人力资源专员/助理
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职位描述

招聘人数:1 人

                职位职责:
                
Provide support to study team as applicable.
Responsible for completeness, quality, tracking, and accessibility of Central Files.
Responsible for accuracy of coded documents/naming conventions for central files.
Provide Clinical Lead and the team with detailed information on study procedures and study related materials.
Ensure adherence to Good Clinical Practice, applicable regulatory and legal
requirements as well as PAREXELs or clients SOPs.
Responsible for up to date reports of study status in CTMS or client equivalent.
Support Functional Leads in the set-up and maintenance of systems e.g. PMED.
Organize project meetings and taking of minutes.
Proactively flag and escalate any project related issues.
Ensure CRF pages are being processed, tracked and forwarded to Data Management on time.
Have up to date knowledge on study procedures and study related materials.
Serve as a resource for the project team or Clinical team, depending on workload can be delegated to other project related tasks (e.g. set-up activities, other).
Recommend process improvements for Clinical Research Assistant tasks.
Contribute to the smooth running of the department and departmental activities e.g. arranging meetings and travel.

Job Qualifications
Skills
Excellent interpersonal, verbal and written communication and customer service skills.
Ability to communicate directly with study team members in an international environment.
Ability to communicate directly with Sponsor / other vendors.
A flexible attitude with respect to work assignments, new learning and travel.
Demonstrated ability to manage multiple and varied tasks with positive attitude, prioritize workload with attention to detail and within agreed timescales.
Willingness to work in a matrix environment and to value the importance of teamwork.
Demonstrated ability to work independently and use initiative to complete tasks.
IT literate – Experience with Microsoft based applications and general knowledge of PC functions, especially knowledge of Excel.

Education
Minimum education – high school diploma – ideally degree in life science, nursing qualification or other related background.
Language Skills
Competent in oral and written English and the local language.
Minimum Work Experience
Previous involvement as CRA assistant in an international study or similar experience in office management of international trial or other related experience would be preferred.
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工作地点

上海 上海市

精鼎医药研究开发(上海)有限公司

公司简介

精鼎医药(PAREXEL International)是全球顶尖的药物研究合同委托机构(CRO),总部位于美国生物医药圣地马萨诸塞州的波士顿附近,在世界各地的 51个国家和地区设有85个分支机构,并拥有超过18,750 名员工,其中亚太地区包括台湾, 韩国,中国(北京,上海,成都,广州,沈阳),香港,印尼,泰国,马来西亚,新加坡,澳大利亚,印度,日本,菲律宾和越南等设有分公司或办事处。 精鼎医药(PAREXEL International)成立于1982年,在三十多年的历程中,一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商,并且取得了卓越成果。目前,我们能够提供全世界CRO领域最为全面的新药临床阶段研发服务,服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案,可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。药物开发流程是一段艰辛的旅程,从新分子实体到药物审批上市后的生命周期及法规管理,每一步都复杂而充满挑战,任何一步的小失误都有可能导致整个流程的失败。精鼎医药凭借三十多年的药物开发经验,在将其顶尖的人才、流程和技术优势汇集到一起的基础上,为客户提供真正一体化的解决方案,可以让您顺利的通过药物开发的各个阶段,简化您旅程的每一步,大大提高成功率。精鼎医药(PAREXEL International)重视与客户的承诺,更重视人才的培育和养成,我们提供完整的教育训练、职涯规划、优于市场的薪资福利、良好工作环境,期许同仁与公司一同成长,迈向未来。  Vision 愿景 一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商。  Mission 发展使命 结合我们的专业知识、经验和创新实力,将会推动生物制药和医疗器械行业在预防和治疗疾病方面取得全球性的成功

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北京大杰致远信息技术有限公司 公司地址:北京市朝阳区来广营中街甲一号朝来高科技产业园二期3A#1-3层 联系方式:010-50916789