Senior Business Systems Analyst-center For Clinical Research Management

Osuphysicians

Columbus, OH, USA
Clinical trial management systems expertise
Electronic health records knowledge
Fda 21 cfr part 11 compliance
The Senior Business Systems Analyst provides subject matter and technical expertise in clinical research operations and informatics to support and enhance IT applications integral to the research mission of The Ohio State University College of Medicine

Job Summary

  • The Senior Business Systems Analyst provides subject matter and technical expertise in clinical research operations and informatics to support and enhance IT applications integral to the research mission of The Ohio State University College of Medicine.
  • This role manages daily oversight of Clinical Research Informatics-supported applications, coordinates with vendors and clinical teams, and ensures compliance with FDA regulations.
  • The position involves leading cross-functional collaboration, developing strategic plans for system upgrades, and providing training and guidance as a subject matter expert.

Matching Summary

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

Skills & Requirements

Must-have

  • clinical trial management systems expertise
  • electronic health records knowledge
  • FDA 21 CFR Part 11 compliance
  • clinical research informatics operations
  • user access administration and audits
  • cross-functional team collaboration

Nice-to-have

  • business intelligence tools experience
  • clinical trial data visualization
  • workflow and user documentation development
  • technical and end-user requirements gathering
  • experience with electronic data capture systems

Key Requirements

  • Bachelor's degree or equivalent experience
  • 4 years of relevant experience required
  • Knowledge of clinical trial workflows and protocols
  • Experience with regulatory affairs and CRF development
  • Preferred advanced degree in relevant field
  • Preferred 4-8 years clinical research experience

Work Rights

Not specified

Tailored Resume

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