临床试验管理证书
的 临床试验管理证书 在 药学院 at 皇冠体育 is specifically designed for pharmaceutical and healthcare professionals who actively contribute to the clinical trial process, 包括医生, 临床研究监测器, 调查人员和协调员, or members of investigational review boards (IRBs). This certificate is part of the 药学院’s regulatory affairs (RA) and quality assurance (QA) graduate program.
This graduate program provides the tools and information needed to understand the basis for new drug discovery, the design and implementation of the clinical protocol, 其行为和有效的监测战略, and the auditing of data to ensure the integrity of the trial. 特定课程强调协议开发, the bioethics of clinical research and the protection of the human research subject, 知情同意书及程序, 临床操作, and the role and responsibilities of the key personnel—the IRB, 赞助商, 监控, contract research organization (CRO) and the clinical investigator.
的 临床试验管理证书 enables students to sharpen their knowledge of clinical trials in a graduate program setting without committing to the entire master’s degree. It provides the tools and information to understand how clinical trials must be designed and overseen 在 pharmaceutical industry, 包括撰写协议和同意书, delving into the requirements of good clinical practices, 管理预算和数据.
更多的 than 60 courses are offered online in real time. 的 临床试验管理证书 may be pursued entirely online. Candidates must complete the required courses and application procedures to receive the certificate.