Role Description
The Oncore Training Specialist is dedicated to supporting the effective utilization, adoption, and optimization of the OnCore Clinical Trial Management System (CTMS) across the University research enterprise. The OnCore Training Specialist plays a crucial role in developing, delivering, and maintaining training and educational programs that support research staff, faculty, and operational stakeholders throughout the clinical research lifecycle.
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Develops, delivers, and maintains training programs and educational materials supporting utilization of the OnCore Clinical Trial Management System (CTMS).
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Creates and updates user guides, standard operating procedures, job aids, reference materials, presentations, and other educational resources related to OnCore functionality and workflows.
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Coordinates onboarding and role-based training activities for clinical research personnel.
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Partners with department leadership to assess evolving training needs and designs strategic educational programs for system enhancements.
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Serves as a subject matter expert for OnCore and related integrations (EPIC, AURA, Oracle, Vestigo).
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Collaborates with system administrators, operational teams, and stakeholders to support implementation of new functionality, workflow enhancements, and system optimization efforts.
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Participates in testing and validation activities associated with system upgrades, enhancements, and new functionality.
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Maintains training environments and develops training scenarios to support hands-on educational activities.
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Develops and maintains workflow documentation and training resources to promote consistent utilization of clinical research systems and processes.
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Tracks training participation, completion metrics, and educational outcomes; develops reports to support operational decision making and continuous improvement activities.
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Communicates system updates, process changes, and educational opportunities to research teams and institutional stakeholders.
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Supports audits, quality assurance activities, and process improvement initiatives related to clinical research systems and operational workflows.
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With some direction from others, performs a variety of IT activities supporting an e-learning environment, such as designing curriculum content.
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Monitors and analyzes trends, identifies opportunities, and explores innovative approaches to teaching and learning problems.
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Performs other related work as needed.
Qualifications
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Minimum requirements include a college or university degree in related field.
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Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
Preferred Qualifications
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Bachelor's degree.
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Proficiency with the Clinical Trial Management System, Oncore, and related research technologies.
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Knowledge of clinical research operations and the clinical trial lifecycle.
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Familiarity with federal regulations governing human subject research.
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Proficiency with Microsoft Office applications including Word, Excel, PowerPoint, and Teams.
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Ability to develop reports, analyze metrics, and evaluate training effectiveness.
Preferred Competencies
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Communicate complex technical concepts to audiences with varying levels of system knowledge.
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Strong presentation, facilitation, and instructional skills.
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Problem-solve, leveraging information and expertise available.
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Strong organizational skills.
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Manage projects at various stages of completion.
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Demonstrated attention to detail.
Working Conditions
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Office environment/Remote.
Application Documents
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Resume (required)
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Cover Letter (required)
Job Family
Role Impact
Scheduled Weekly Hours
Pay Rate Type
FLSA Status
Pay Range
Benefits
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The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off.