Senior Business Systems Analyst - Comprehensive Cancer Center

The Ohio State University

Completely RemoteFull TimeHealthcare & Telemedicine
Posted Today

Job description

Responsibilities

  • Oversee daily operation and troubleshooting of CRI-supported applications
  • Manage user access, conduct audits, and document standard operating procedures
  • Coordinate with vendors and informatics engineers to test and implement new modules
  • Ensure compliance with FDA 21 CFR Part 11 and other regulatory standards
  • Facilitate cross-functional collaboration between IT, research billing, and clinical trials offices
  • Develop strategic plans for system upgrades across the Clinical Research Informatics environment
  • Create and maintain formal training manuals and procedures for end users
  • Collect data requirements for research protocol reporting and data visualization tools

Requirements

  • Bachelor's degree in health science or equivalent experience in clinical research operations
  • 4 to 8 years of relevant clinical experience in a clinical research setting
  • Expertise in clinical trial workflows, data requirements, and regulatory affairs
  • Proficiency with clinical trial management systems (CTMS) and electronic health records (EHR)
  • Knowledge of case report form (CRF) development and protocol development

Preferred Qualifications

  • Advanced degree in a relevant field
  • Knowledge of business intelligence tools such as Excel, Tableau, or Power BI
  • IT work experience involving technical requirement gathering
  • Experience developing workflows and user documentation

About the Company

The Ohio State University is a top-20 public university and home to one of America's leading academic health centers, dedicated to excellence in education, research, and healthcare.

Skills & tools

Clinical ResearchCTMSEHR

What the team is looking for

Use this list as a quick fit check before you apply.

  1. 01Bachelor's degree in health science
  2. 024 to 8 years clinical research experience
  3. 03Expertise in clinical trial workflows
  4. 04Knowledge of regulatory affairs (FDA 21 CFR Part 11)
  5. 05Experience with CTMS and EHR systems
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