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Responsible for the development, maintenance and adherence to Genmab’s clinical data standards including eCRFs, edit checks, electronic case report forms (eCRFs) Completion Guidelines, controlled terminology, CDISC, CDASH and etc. The Associate Director
Provide epidemiology and statistical analytical support for RWE studies; Contribute to the development of evidence generation plans and design of RWE studies for scientific and regulatory purposes; Advise study teams on research methodologies and