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Lucienne Augustin

Senior Clinical Regulatory Manager

lucienne-augustinLucienne works closely with sites to ensure regulatory compliance, including collection of each site’s study-specific documents for regulatory readiness and open to accrual. She submits IND applications to the FDA. She submits new study packet information to all participating sites and supports the on-boarding activities of new Hoosier Cancer Research Network member sites. Lucienne is responsible for the renewal and approval of site-specific Informed Consents for IRB submission and provides support for IRB submission of Indiana University studies through the Hoosier Cancer Research Network. She is also a notary public.