卫生专业:临床研究监测和协调

临床研究监测和协调性训练


This online multi-media course provides essential training to meet job requirements in clinical trial monitoring and study management. The course provides key foundation skills and terminology for success and qualification as a clinical research associate (CRA) or clinical re搜索 coordinator (CRC) as well as related CTM, CTS, CPS titles. The course is also ideal for Medical Monitors, Clinical Scientists and Project Managers who want technical and regulatory knowledge of Good Clinical Practice (GCP) related to pharmaceutical R&D. The course is certified through TransCelerate and ANCC organizations, meeting all ICH GCP E6 training requirements and clinical standards for global trial sponsors.

Whether you are seeking your first position in clinical research or need to quickly enhance a detailed knowledge of global GCP standards, this University certificate course uniquely qualifies you in clinical research & development to work directly with study patients or manage the research functions in clinics, hospitals and/or global pharmaceutical companies. Course completion allows you to join the ever-growing demand for trained clinical study professionals in the 搜索 for exciting state-of-art medical cures and therapeutics.

当然亮点

  • 学临床研究药物开发过程和角色/机会
  • 应用和理解良好的临床实践要领
  • 建立高效的对象招募,监测和报告技术
  • 学院并获得适当的知情同意和监管机构批准
  • 确定伦理问题及其对新产品开发的影响
  • 制定了详细的临床试验方案和有效的数据收集方法
  • 敲定研究预算和关键的临床数据管理程序
  • 确定不良足球外围官网和适当的报告标准
  • 农产品研究分析报告和最终报告
  • 检验学习审计和检查,以及各种申办者 - 研究者实地考察
  • 采用实际监管事务方法来研究审批,审核和备案
  • 学生完成时间为两个星期至四个月。

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当然#alh 170 900

  • 滚动登记:在线多媒体,自学课程,24-7访问和支持任何智能手机,平板电脑,笔记本电脑或台式电脑上
  • 所在位置:在线
  • 费用:$ 1,975
  • Instructor: John F. Arditi, B.S., M.S., R&D Executive and Consultant
  • 当然管理员:朱丽叶湖惠特利。请直接课程内容或职业相关的问题juliet.wheatley@delval.edu。

这ICH GCP E6调查现场培训,以满足生物制药transcelerate INC培训确定了ICH GCP调查现场工作人员的标准。根据需要,使审判赞助商之间的GCP培训的互认。

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