更新于 12月24日

武汉-临床数据协调员

8000-11000元
  • 武汉武昌区
  • 1-3年
  • 本科
  • 全职
  • 招1人

职位描述

临床数据分析
Responsibilities:
  1. CRF/DCF tracking;
  2. Develop test scripts and execution logs for User Acceptance Testing (UAT);
  3. Database audit;
  4. Perform data review;
  5. Create and maintain Data Management Plan under the supervision of senior members;
  6. Create and maintain Data Validation Plan under the supervision of senior members;
  7. Create and maintain Data Entry Guidelines;
  8. Create Data Handling Plan under the supervision of senior members;
  9. Create Data Transfer Specification under the supervision of senior members;
  10. Perform CRF design and CRF review under the supervision of senior members;
  11. Develop database (DB) clinical trial data specifications under the supervision of senior members, including eCRF design, user requirements, edit rules/checks, query logic and data validations.
  12. Perform SAE reconciliation;
  13. Perform external data reconciliation in collaboration with programmers;
  14. Other DM tasks as deemed appropriate by senior members.
  15. Other activities/tasks assigned by supervisor.
Qualification:
  1. Bachelor’s degree in clinical/pharmacy/biological/mathematical sciences or related field or nursing degree with 1-3 year clinical experience.
  2. Working knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.
  3. Good understanding of clinical drug development process.

工作地点

武汉武昌区公正路216号

职位发布者

刘女士/TAM

昨日活跃
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公司Logo昆翎(北京)医药科技发展有限公司
昆翎(ClinChoice)是一家致力于为生物医药和医疗器械客户提供高品质一站式服务的临床阶段CRO,服务包括临床运营、项目管理、生物统计、数据管理、注册事务、医学事务和药物警戒。昆翎已经在中国、美国、欧洲、印度、日本和菲律宾建立了主要的临床交付中心,目前在全球拥有1800多名员工,其临床运营团队覆盖了亚、欧、北美等七个国家和地区。高盛直投部董事总经理、昆翎董事会成员许小鸥先生认为,“随着创新疗法在全球的增长,CRO公司提供高效、可靠的研发服务能力变得尤其重要。昆翎独特的价值主张结合了其对于本地市场的了解、国际药物研发的经验以及高效的团队执行能力。我们坚信公司强劲的管理层团队以及其高效的执行能力,将为昆翎的发展开启新的篇章。
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