University of Chicago

Oncore Training Specialist

University of Chicago$70K — $100K *
US-AnywhereRemote in Chicago, IL
Education, Government & Non-Profit
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a related field (preferred)
  • 2-5 years of relevant work experience
  • Proficiency in the OnCore Clinical Trial Management System
  • Knowledge of clinical research operations and the clinical trial lifecycle
  • Familiarity with federal regulations governing human subjects research
  • Strong proficiency in Microsoft Office applications
  • Ability to analyze metrics and evaluate training effectiveness

Responsibilities

  • Develop training programs and materials for OnCore CTMS utilization
  • Create and update guides, procedures, and educational resources
  • Coordinate onboarding and ongoing training for clinical research staff
  • Collaborate with leadership to assess training needs and design programs
  • Serve as a subject matter expert on OnCore and related technologies
  • Participate in testing and validation related to system enhancements
  • Monitor training metrics and develop reports for continuous improvement

Benefits

  • Wide range of health benefits
  • Retirement plan options
  • Paid time off
  • Access to employee resources and support programs
Full Job Description

Department

BSD OCR - Operations Infrastructure Support


Job Summary

The job provides professional support and solves straightforward problems in the development, deployment, and support of information technology products and services used in teaching and learning.

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. As a member of the Research Systems & Coverage Analysis (RSCA) Unit within the Office of Clinical Research, the OnCore Training Specialist works as part of a team to support and optimize clinical research operations, partnering closely with research teams and key stakeholders throughout the institution.

The OnCore Training Specialist serves as a subject matter resource for OnCore and related research technologies, helping advance system adoption, data quality, compliance, and operational effectiveness while promoting standardized research workflows and best practices.

Responsibilities

  • Develops, delivers, and maintains training programs and educational materials supporting utilization of the OnCore Clinical Trial Management System (CTMS).

  • Creates and updates user guides, standard operating procedures, job aids, reference materials, presentations, and other educational resources related to OnCore functionality and workflows.

  • Coordinates onboarding and role-based training activities for clinical research personnel.

  • Partners with department leadership to assess evolving training needs and designs strategic educational programs for system enhancements, ensuring all delivery methods remain current, effective, and aligned with process changes.

  • Serves as a subject matter expert for OnCore and related integrations (EPIC, AURA, Oracle, Vestigo), providing guidance and support to end users.

  • Collaborates with system administrators, operational teams, and stakeholders to support implementation of new functionality, workflow enhancements, and system optimization efforts.

  • Participates in testing and validation activities associated with system upgrades, enhancements, and new functionality.

  • Maintains training environments and develops training scenarios to support hands-on educational activities.

  • Develops and maintains workflow documentation and training resources to promote consistent utilization of clinical research systems and processes.

  • Tracks training participation, completion metrics, and educational outcomes; develops reports to support operational decision making and continuous improvement activities.

  • Communicates system updates, process changes, and educational opportunities to research teams and institutional stakeholders.

  • Supports audits, quality assurance activities, and process improvement initiatives related to clinical research systems and operational workflows.

  • With some direction from others, performs a variety of IT activities supporting an e-learning environment, such as designing curriculum content.

  • Monitors and analyzes trends, identifies opportunities, and explores innovative approaches to teaching and learning problems. Works with other units across campus to aggregate services in an academic context.

  • Performs other related work as needed.


Minimum Qualifications

Education:

Minimum requirements include a college or university degree in related field.


Work Experience:

Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.


Certifications:

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Preferred Qualifications

Education:

  • Bachelor's degree.

Experience:

  • Proficiency with the Clinical Trial Management System, Oncore, and related research technologies.

  • Knowledge of clinical research operations and the clinical trial lifecycle.

  • Familiarity with federal regulations governing human subject research.

  • Proficiency with Microsoft Office applications including Word, Excel, PowerPoint, and Teams.

  • Ability to develop reports, analyze metrics, and evaluate training effectiveness.

Preferred Competencies

  • Communicate complex technical concepts to audiences with varying levels of system knowledge.

  • Strong presentation, facilitation, and instructional skills.

  • Problem-solve, leveraging information and expertise available.

  • Strong organizational skills.

  • Manage projects at various stages of completion.

  • Demonstrated attention to detail.

Working Conditions

  • Office environment/Remote.

Application Documents

  • Resume (required)

  • Cover Letter (required)


The University of Chicago uses AI-assisted tools to streamline and augment some recruitment processes; however, AI is not used to make hiring decisions.

When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.


Job Family

Information Technology


Role Impact

Individual Contributor


Scheduled Weekly Hours

40


Drug Test Required

No


Health Screen Required

No


Motor Vehicle Record Inquiry Required

No


Pay Rate Type

Salary


FLSA Status

Exempt


Pay Range

$70,000.00 - $100,000.00

The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.


Benefits Eligible

Yes

The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in theBenefits Guidebook.

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