Hands-on monitoring fundamentals: oversight, on-site & remote visits, documentation, drug accountability, AE reporting, audit readiness, and close-out — with live Q&A.
Aligned to ICH-GCP and FDA standards. Practical monitoring demos included.
“The webinar clarified how to conduct on-site monitoring and manage drug accountability logs effectively. I was able to add these skills to my resume and landed my first CRA/CTM interview.”
— Michael T., Boston, USA“Learning about AE reporting and audit readiness helped me transition from a Clinical Research Coordinator to a monitoring role. The examples on documentation were especially practical.”
— Sophie L., Vancouver, Canada“The session gave me confidence in handling monitoring visits and source document verification. I now feel ready to apply for Clinical Trial Monitor positions in CROs.”
— Rahul K., Hyderabad, IndiaClinical Operations Expert · 25+ years in the Pharmaceutical Industry
Dr. Nate is a seasoned leader in Clinical Operations, LMS, and Clinical Technology Systems with hands-on expertise in CTMS/eTMF, Drug Safety, Pharmacovigilance, Oracle Argus, Veeva eTMF, Medidata RAVE & CTMS, Risk-Based Monitoring, SAS Data Analytics, and Regulatory Compliance. He has trained and mentored hundreds of professionals globally.
Known for bridging technology with clinical trial execution, Dr. Nate empowers Clinical Trial Monitors and site teams with job-ready skills.