Institutional Review Board (IRB)

您将获得的技能: 感染控制, 安全培训, 持续质量改进 (CQI), 患者安全, 重症监护室, 风险管理, 护士教育, 机构审查委员会（IRB）

您将获得的技能: 质量保证, 数据收集, 监管合规, 临床数据管理, 数据清理, 知情同意, 数据完整性, 数据输入, 临床试验, 数据质量, 样本量的确定, 临床文件, 临床研究, 良好临床实践（GCP）, 统计报告, 病例报告表, 临床研究伦理, 临床试验管理系统, 数据管理, 机构审查委员会（IRB）

您将获得的技能: Good Clinical Practices (GCP), Informed Consent, Institutional Review Board (IRB), Clinical Research Ethics, Clinical Research Coordination, Clinical Research, Clinical Trials, Clinical Data Management, Drug Development, Patient Education And Counseling, Record Keeping, Clinical Documentation, Regulatory Compliance, Document Management, Health Equity, Electronic Medical Record, Patient Communication, Risk Management

您将获得的技能: 冲突管理, 数据分析, 纠正和预防措施 (CAPA), 解决方案设计, 风险分析, 系统思考, 设计思维, 项目规划, 风险管理, 持续质量改进 (CQI), 管理团队, 变革管理, 基于价值的护理, 患者安全, 质量改进, 绩效衡量, 卫生系统, 数据分析软件, 以患者为中心的护理, 机构审查委员会（IRB）

您将获得的技能: Institutional Review Board (IRB), Clinical Trials, Health Policy, Health Disparities, Clinical Research, Clinical Research Ethics, Health Equity, Healthcare Ethics, Public Health, Epidemiology, Good Clinical Practices (GCP), Pre-Clinical Development, Policty Analysis, Research, and Development, Health Care, Medical Science and Research, Policy Development, Health Care Procedure and Regulation, Community Health, Drug Development, Research

您将获得的技能: Data Ethics, Data Sharing, Personally Identifiable Information, Clinical Research Ethics, Institutional Review Board (IRB), Healthcare Ethics, Data Security, Data Governance, Information Privacy, Health Insurance Portability And Accountability Act (HIPAA) Compliance, Health Information Management, Informed Consent, Encryption