Clinical Trials System Administrator

Responsibilities

• Perform in-depth analysis of research operation workflows and data collection methods.
• Create workflow diagrams and step-by-step process documentation.
• Identify opportunities for process optimization and implement solutions.
• Participate in the integration efforts between the Network Clinical Trials Management System and other clinical operating systems (i.e. EPIC).
• Consult and collaborate with the clinical research management teams to review reporting needs.
• Prepare reports and dashboards; run ad hoc queries.
• Affiliate in testing and system validation.

Qualifications/Requirements

• Experience: Five years of experience in systems analysis and application program development.
• Proficient in Microsoft Excel.
• Knowledge of Microsoft Visio preferred.
• Knowledge of Tableau preferred.
• Knowledge of OnCore/Clinical Trials Management Systems preferred.
• Knowledge of EPIC preferred.