This position is responsible for securely managing information systems throughout their lifecycle, including; knowing what information systems are within their scope of responsibility, understanding what sensitive data is stored, transmitted, or processed on those information systems, enforcing the security principles of least privilege and least functionality, knowing what events may constitute an information security incident, and understanding their role in security incident response activities.
The Clinical Research Application Analyst 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. The Clinical Research Application Analyst will support and administer future technologies as required. Come join a remarkable team where quality care meets quality service, in every dimension, every time.
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At Novant Health, one of our core values is diversity and inclusion. By engaging the strengths and talents of each team member, we ensure a strong organization capable of providing remarkable healthcare to our patients, families and communities. Therefore, we invite applicants from all group dynamics to apply to our exciting career opportunities.
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