Title Level Category
Benefit-risk assessment and pharmacovigilance Beginner Clinical Trial Management
Clinical Trials Information System (CTIS) Beginner Clinical Trial Management
Clinical Trials Operations Specialization Beginner Clinical Trial Management
CONSCIOUS I Curriculum Chapter 13: Adverse events and reporting responsibilities Beginner Clinical Trial Management
CONSCIOUS I Curriculum Chapter 5: What patients should know _ informed consent Beginner Clinical Trial Management
CONSCIOUS I Curriculum Chapter 9: The clinical trial protocol & case report forms (CRF) Beginner Clinical Trial Management
CONSCIOUS II Curriculum Chapter 10 - Leadership for 21st Century Trialists Intermediate Clinical Trial Management
CONSCIOUS II Curriculum Chapter 3 - Trial Management Intermediate Clinical Trial Management
CONSCIOUS II Curriculum Chapter 4 - Quality and Regulatory Affairs Intermediate Clinical Trial Management
CT Regulations/Ethics
CONSCIOUS II Curriculum Chapter 5 - Pharmacovigilance and Study Medication Intermediate Clinical Trial Management
CONSCIOUS II Curriculum Chapter 6 - Data Management and Statistical Analysis Intermediate Clinical Trial Management
CTMC 2021 Webinar Series: Adverse Event and Safety Reporting Intermediate Clinical Trial Management
CTMC 2021 Webinar Series: Trial Management Beginner Clinical Trial Management
Data Management for Clinical Research Beginner Clinical Trial Management
International Program for site staff conducting clinical research Beginner Clinical Trial Management
Introduction to the Principles and Practice of Clinical Research (IPPCR) Beginner Clinical Trial Management
Master Your Clinical Trial Budget:A Step-by-Step Guide to Smart Clinical Expense Planning Intermediate Clinical Trial Management
Safety in Clinical Trials Beginner Clinical Trial Management
Safety Management in Clinical Research. Medical Devices Beginner Clinical Trial Management
Site Management Modules Beginner Clinical Trial Management