Senior Business Systems Analyst-center For Clinical Research Management

Ohio State University Physicians Inc

Columbus, Ohio, US
Clinical trial management system
Electronic health records
Fda 21 cfr part 11 compliance
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 planning, development, integration, 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
  • electronic health records
  • FDA 21 CFR Part 11 compliance
  • clinical research operations
  • system vendor coordination

Nice-to-have

  • strategic planning for system upgrades
  • cross-functional collaboration
  • end-user system training
  • data visualization tools

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 development
  • Expertise in protocol development

Work Rights

Not specified

Tailored Resume

Cover Letter