Research Assistant III (Lab) (4116)

Conduct patient visits and assist in collecting, managing, and shipping subject samples while maintaining accurate records in the EDC system. Complete required training on GCP, IATA, and sponsor protocols before study start, and report adverse events to appropriate authorities. Assist in addressing audit findings, organizing regulatory binders, and creating source documents for assigned protocols. Maintain working knowledge of FDA regulations and organizational SOPs. Available for company meetings and monitoring visits at respective sites.