Master CRC essentials: protocol & site start-up, participant recruitment & consent, data & source documentation, safety reporting, audits — with live Q&A.
Aligned to ICH-GCP and regulatory frameworks; real-site scenarios included.
“The CRC webinar clearly explained participant recruitment and informed consent. I applied these steps at my site and was commended by my PI for improved documentation.”
— Emily S., Chicago, USA“The hands-on examples for source documentation and safety reporting gave me confidence in managing site visits. I was able to transition into a CRC role at a CRO.”
— Lucas M., Toronto, Canada“Learning about audits, data entry accuracy, and AE reporting helped me understand real CRC responsibilities. I now feel job-ready and prepared for clinical site positions.”
— Priya K., Bengaluru, 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, safety, PV, monitoring, and regulatory compliance. He has trained and mentored professionals worldwide.