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Clinical Trials Resource Center

Clinical Research Training

Human Subjects Training via CITI Program- 所有临床研究研究人员和研究人员需要每3年每3年。beplay苹果手机能用吗可用的课程是：

  • Group 1 Biomedical Researcher and Key Personnel
  • Group 2 Social and Behavioral Researchers and Key Personnel
  • Social & Behavioral Educational Researchers (SBR) - Spanish
  • Biomedical Researchers - Spanish

Good Clinical Practice (GCP) Course via CITI Program- 临床试验研究人员和研究人员需要每3年每3年。beplay苹果手机能用吗可用的课程是：

  • Good Clinical Practice
  • GCP for Social and Behavioral Research Best Practices for Clinical Research
  • GCP（美国FDA焦点） - 西班牙语

Informed Consent Training - Mandatory- All research staff involved in the informed consent (coordinators and nurses) process must have informed consent training. This training will be in addition to the CITI human subjects training. This is a one-time training requirement. Continuing education is encouraged but not required under this policy.

临床研究人员的方向beplay苹果手机能用吗– The clinical research staff orientation is a fully online program。该计划将涵盖CPHS（UTHealth IRB）审查和批准过程，纪念Hermann医院审查和批准过程以及临床试验管理的基础知识。演示文稿已被记录，您可以在您自己的时间观看。

Clinical Coordinator Forum-This monthly meeting is open to all coordinators, nurses, administrators 和investigators involved in clinical research. The meeting provides both an opportunity for education and information sharing among research personnel. Presentations highlight best practices and ethical considerations in clinical research management to engage dialogue and problem-solving among research practitioners.

iRIS Training-The first half of the session provides participants with an overview of completing the initial IRB application and routing and sign-off process. The second half of the class provides an overview on responding to "pending issues" when a submission is returned to the study team.

Clinical Research Education Course - Basic- The clinical research education course is offered every year in the Fall. This course covers good clinical practice guidelines from study start up, regulatory reviews, study initiation, study conduct until study closure. Registration for this course usually opens in August.

Infectious Substances Shipping Training- 这项培训是由安全，健康，环境和风险管理团队进行的。对于处理和运送人类生物标本的研究人员需要每2年一次。beplay苹果手机能用吗

ADDITIONAL RESOURCES

CLINICAL RESEARCH UNITS (CRU)|伯德|REDCap
COMMITTEE FOR THE PROTECTION OF HUMAN SUBJECTS|ANIMAL RESEARCH|ENVIRONMENTAL HEALTH & SAFETY|CORE LABORATORIES|赞助项目|TECHNOLOGY MANAGEMENT
OFFICE OF RESEARCH

Center for Clinical and Translational Sciences

Clinical Trials Resource Center (CTRC)
7000 Fannin Street，Suite 795
德克萨斯州休斯顿77030
phone 713-500-3622
fax 713-500-0334
clinicaltrials@uth.tmc.edu

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