Senior Business Systems Analyst – Comprehensive Cancer Center

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee daily operations and management of CRI-supported applications

• Handle troubleshooting, manage user access control and administration, conduct access audits, and document standard operating procedures

• Collaborate with system vendors, clinical research operations, and informatics engineers to test, validate, and deploy new or updated Clinical Research Enterprise modules

• Revise validation documentation and Standard Operating Procedures to ensure compliance with FDA 21 CFR Part 11 and other relevant regulations

• Lead and promote cross-functional teamwork among clinical research, information technology, research billing, and clinical trials offices

• Engage in strategic planning for system upgrades and implementations within the Clinical Research Informatics landscape

• Provide technical contributions to the planning, development, integration, and support of OSUMC Clinical Research Enterprise systems

• Develop, implement, and maintain formal training manuals and procedures, collaborating with end-user training teams

• Offer guidance and act as a subject matter expert for colleagues

• Supervise the collection of data requirements for clinical trial reporting, system notifications, and data visualization tools

• Work with data managers and clinical trials subject-matter experts to prepare data for significant initiatives and NIH and NCI grants

• Interact with principal investigators, clinical research staff, and OSU committees related to the Institutional Review Board

⛳️ Requirements

• Bachelor's degree in health science; advanced degree preferred, or a combination of education and experience in clinical trials management systems or clinical research operations

• Four to eight years of pertinent clinical experience in a clinical research environment

• Expertise in clinical trial workflows and the ability to navigate complex protocols

• Proficiency in clinical trial data requirements, regulatory affairs, case report form (CRF) development, and protocol development

• Familiarity with clinical trial management systems and electronic health records

• Exceptional oral and written communication, facilitation, and consensus-building skills

• Capability to work independently

• Knowledge of business intelligence tools and report formatting applications such as Excel, Tableau, and Power BI is preferred

• Preferable IT work experience

• Experience in gathering and understanding technical and end-user requirements is beneficial

• Experience in developing workflows and user documentation is an advantage

• Understanding of principal investigator and clinical research staff roles within a medical center’s clinical research enterprise

• Involvement with key committees linked to the Institutional Review Board (IRB)

• Final candidates will be subject to a successful background check

• A drug screen or physical may be necessary during the post-offer process

🏝️ Benefits

• Medical, dental, and vision coverage, with Ohio State covering a substantial portion of the cost

• Paid time off, including vacation and sick leave, plus 11 holidays

• State retirement plan or an alternative retirement plan, both with generous employer contributions

• Comprehensive benefits starting from day one

• Access to extensive resources that support employees

• Opportunities for growth across various fields and specialties