Senior Business Systems Analyst-center For Clinical Research Management
The Ohio State University
Columbus, OH, US
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 to implement system updates, and ensures compliance with FDA regulations.
The position leads cross-functional collaboration across the clinical research enterprise and participates in strategic planning for system upgrades and implementations.
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 applications
user access administration and audits
cross-functional team collaboration
Nice-to-have
business intelligence tools experience
clinical trial workflows expertise
technical and end-user requirements gathering
workflow and user documentation development
training manual creation and maintenance
Key Requirements
Bachelor's degree or equivalent experience
4 years relevant clinical research experience
subject matter expertise in clinical trial workflows
knowledge of regulatory affairs and protocol development
experience with clinical trial data requirements
ability to navigate complex clinical trial protocols