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  1. Clinical Trials Quality Director - Danbury, CT

    Seeking at least 5 years directing and coordinating quality assurance activities for good clinical practices, coordinate and oversee inspections to ensure compliance to FDA regulations, IRB and IEC regulations and guidelines, site SOPs, protocols, and industry standards. Shall: *** Direct and coordinate GCP quality assurance activities. *** Author GCP documentation: protocols, case report forms, tables, listings, reports, and investigational brochures. *** Plan and execute document audits and ...