Level up CRA skills: RBM strategy, KRIs/dashboards, deviations & CAPA, eTMF quality, cross-functional leadership, and mentoring — plus regulatory updates and career transitions.
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Aligned to ICH-GCP E6(R2/R3) and global regulatory expectations.
“The webinar gave me clarity on managing protocol deviations and CAPA at a global trial level. I updated my resume with advanced CRA tasks and was shortlisted for a Senior CRA position.”
— Jessica M., Dallas, USA“Learning how to use KRIs and dashboards for Risk-Based Monitoring made me much more confident in trial oversight. These insights helped me move from CRA to Lead CRA responsibilities.”
— Ryan P., Ottawa, Canada“Hands-on examples in eTMF quality review and inspection readiness gave me the confidence to handle audits. I now feel ready to transition into Clinical Study Manager roles.”
— Neha S., Mumbai, 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 equips ACRAs with job-ready skills across complex, global studies.