Comprehensive Role-Based Training for Clinical Research Professionals
Barnett International's Core Curriculum courses are comprehensive role-based clinical research training programs designed to provide industry professionals with hands-on training in a dynamic virtual setting. Held four times a year during our “Clinical Research Training Weeks,” courses offer clinical research-focused, performance-based training and core competency development.
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Monitoring Clinical Drug Studies: Intermediate -
Clinical Project Management: Fundamentals of Project Management -
Introduction to Clinical Research -
CRA & CRC: Beginner Program -
Auditing Techniques for Clinical Research Professionals -
Drug Safety and Pharmacovigilance: Effective Drug Safety Reporting and Surveillance -
WORKSHOP: Trial Master Files: Why They Are Important and How to Organize Them -
Clinical Trial Assistant Fundamentals -
Clinical Project Management: Advanced Concepts in Project Management -
Statistical Concepts for Non-Statisticians -
Comprehensive Monitoring for Medical Devices -
Monitoring Clinical Drug Studies: Beginner -
Monitoring Clinical Drug Studies: Advanced -
Clinical Trial Start-Up: Effective Planning for Sponsors, CROs, and Sponsor-Investigators -
Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) in Site Management -
Conducting Clinical Trials Under ICH GCP E6 -
Clinical Project Management: Fundamentals of Project Management -
Introduction to Clinical Research -
Monitoring Clinical Drug Studies: Beginner -
Clinical Trial Start-Up: Effective Planning for Sponsors, CROs, and Sponsor-Investigators -
Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) in Site Management -
Monitoring Clinical Drug Studies: Intermediate -
Comprehensive Monitoring for Medical Devices -
Monitoring Clinical Drug Studies: Advanced
