Learn CRA fundamentals: ICH-GCP essentials, site selection & initiation, SDV/SDR basics, essential documents, visit reporting, and professional communication — with live Q&A.
Aligned to ICH-GCP E6, FDA and regulatory guidelines; modern clinical trial best practices.
“Clear overview of ICH-GCP and TMF expectations. I felt prepared for site initiation and monitoring basics.”
— Avery L., Philadelphia, USA“Practical walkthroughs of consent documentation and visit reports helped me structure my notes better.”
— Lucas R., Calgary, Canada“The focus on AE documentation and audit readiness connected classroom learning to real CRA tasks.”
— Rhea S., Chennai, IndiaClinical Operations Expert · 25+ years in the Pharmaceutical Industry
Dr. Nate is a seasoned leader in Clinical Operations and Technology Systems with hands-on expertise across CTMS/eTMF, monitoring, TMF, and regulatory compliance. He has trained and mentored hundreds of professionals, focusing on practical, job-ready CRA skills you can apply from day one.