Research Regulatory Specialist

Research Regulatory Specialist responsible for ensuring timely submission of complete, accurate regulatory documents to sponsors, IRB, and CROs; maintain and update regulatory documents, delegation logs, and staff qualifications; assist with study start-up activities (site contact questionnaires, imaging questionnaires, qualifications), ensure proper consents/re-consents, and maintain training records (GCP/HSP, IATA, CPR); ensure compliance with federal regulations and ICH-GCP; oversee initiation, monitoring, closeout, and audit visits and assist with IND safety reports; requires attention to detail, strong organization, proficiency in Microsoft Office, ability to work autonomously, and effective written/verbal communication; associates degree or two years healthcare/research experience required; location Chandler, AZ; full-time.