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Comprehensive Curriculum
Gain in-depth knowledge and practical skills in clinical research auditing
Expert Guidance
Learn from industry experts with years of experience in the field
Career Advancement
Boost your career prospects with a training certificate in clinical research monitoring
About the Course
Target Audience
Individuals with prior training and experience as a CRA; Bachelor's degree minimum education requirement
Comprehensive Content
Embark on a transformative journey to become a Clinical Research Professional with our comprehensive course. Dive deep into the world of clinical research monitoring and equip yourself with the necessary skills to excel in this dynamic field.
Active Learning
Our expert-led curriculum is designed to provide you with practical knowledge and hands-on experience, ensuring you are well-prepared for a successful career as a clinical research monitor.
About the Creator
Dr. Alia Legaux is a former U.S. FDA Investigator with more than 24 years of experience monitoring, inspecting and/or auditing of FDA regulated entities, such as Clinical Research Investigator Sites, Clinical Research Organizations (“CROs”), Sponsors, Ethics Committees, Vendors (i.e. safety reporting, laboratory testing, data management, biostatistics, programming, electronic data capture, interactive voice response services, electronic clinical outcome assessments, central reading and imaging), Compounding Pharmacies, Blood Banks, and/or Tissue Banks. As an Independent Consultant, Alia provides expertise in quality assurance and compliance. She conducts domestic and international routine, directed (for-cause), qualification, re-qualification, and inspection readiness audits, as well as mock inspections of investigator sites, CROs, Sponsors, vendors, compounding pharmacies, drug manufacturers, packagers, or labelers to assess compliance with applicable regulations, protocols, investigational plans, Standards Operating Procedures (“SOPs”), International Conference on Harmonization (“ICH”) Good Clinical Practice (“GCP”), Good Manufacturing Practice (“GMP”), Good Laboratory Practice (“GLP”), Good Clinical Laboratory Practice (“GcLP”), and Good Pharmacovigilance Practice (“GVP”).
Start Your Journey Today
Unlock the doors to a successful career in clinical research monitoring. Enroll now and take the first step towards becoming a Clinical Research Professional.
$1,699.00