Wilmington, North Carolina14 days ago
The Clinical Research Application Analyst II will be responsible for administering established clinical research information systems such as the Clinical Trial Management System (CTMS), e-Regulatory platform, interoperability with the health system Electronic Medical Record (EMR) system, electronic signature platforms, provider and consumer-facing research portal interfaces, various internal and external research databases/registries, investigational pharmacy platforms and other systems as required. Regular activities include, but are not limited to, the following: monitoring of clinical research software; troubleshooting and reporting software issues; supporting end-users; supporting software upgrades, managing configuration of software; assisting with implementation of new processes; organizing and maintaining the electronic Trial Master File (eTMF); and liaising with Digital Products and Services (DPS) to support clinical research conduct in information systems.