Senior Business Systems Analyst

The Ohio State University

Columbus, Ohio, USA
Clinical trial management system (ctms)
Electronic data capture system
Regulatory ebinder platform
The Senior Systems Business Analyst provides subject matter and technical expertise in clinical research operations and informatics to support, integrate and enhance information technology applications integral to the research mission of The Ohio State University College of Medicine

Job Summary

  • The Senior Systems Business Analyst provides subject matter and technical expertise in clinical research operations and informatics to support, integrate and enhance information technology applications integral to the research mission of The Ohio State University College of Medicine.
  • Responsibilities include daily oversight and operation of Clinical Research Informatics (CRI)-supported applications, managing troubleshooting, administering user access, conducting audits, and documenting standard operating procedures.
  • The role involves leading cross-functional collaboration with multi-disciplinary teams, participating in strategic planning for system upgrades, and acting as a technical contributor in the development and support of OSUMC Clinical Research Enterprise systems.

Matching Summary

The Senior Systems Business Analyst provides subject matter and technical expertise in clinical research operations and informatics to support, integrate and enhance information technology applications integral to the research mission of The Ohio State University College of Medicine.

Skills & Requirements

Must-have

  • Clinical trial management system (CTMS)
  • Electronic data capture system
  • Regulatory ebinder platform
  • Electronic medical record integrations
  • FDA 21 CFR Part 11 compliance
  • Cross-functional collaboration

Nice-to-have

  • Strategic planning for system upgrades
  • Subject matter expert resource
  • Data visualization tools
  • Collaboration with data managers

Key Requirements

  • Bachelor's degree or equivalent experience
  • 4 years of relevant experience
  • Knowledge of clinical trial management systems
  • Knowledge of electronic health records
  • Expertise in clinical trial data requirements
  • Expertise in regulatory affairs
  • Expertise in case report form (CRF) development
  • Expertise in protocol development

Work Rights

Not specified

Tailored Resume

Cover Letter