Ibukun O.

About Ibukun O.

Ibukun Ogunmodede is a Data Consultant at Deer Brook Consulting, where she partners with the data team to optimize reporting and financial processes for universities. In her role, she works extensively with the Anthology software platform, focusing on financial functions, mastering navigation, and producing detailed reports that support finance production. Leveraging her expertise with SQL, Power BI, and Anthology, she transforms complex datasets into actionable insights, helping clients improve decision-making, streamline operations, and maintain data integrity. Ibukun brings more than six years of experience in data analysis, reporting, and business intelligence. At Microsoft, she served as a Senior Data Analyst, building SQL-based data pipelines in Azure Data Factory, developing interactive Power BI dashboards, and collaborating across teams to enhance reporting speed and accuracy. Her career also includes roles at Charter Communications, where she supported billing product launches and improved deployment efficiency, and at Atrium Health, where she streamlined HIPAA-protected health data reporting. She has also contributed her expertise to Mayo Clinic, Premier, Inc, and other organizations, focusing on data quality, compliance, and process improvement. She is certified as a Tableau Desktop Specialist and a Project Management Professional (PMP). With her combination of technical expertise, analytical skill, and strong communication abilities, Ibukun thrives in roles that require both deep technical knowledge and cross-functional collaboration. Ibukun is a lifelong learner who enjoys taking on new trades and expanding her skills. Her curiosity, adaptability, and dedication to learning reflect the same qualities she brings to her professional work: a drive to explore, innovate, and deliver meaningful results.

Experience

1. Clinical Research Professional

   Clinical Research Fastrack

   Nov 2024 — Present

   Clinical Research Training covering Core Competencies including: ICH GCP E6 R (2) FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 Data Management Informed Consent Process Clinical Trial Operations from feasibility through close-out GDP following ALCOA-C principles Identification and reporting of AEs and SAEs Quality Assurance, Monitoring, and Query Resolution Comprehension and Execution of Clinical Trial Protocols Maintaining a regulatory binder, housing essential documents including but not limited to 1572, DOA, Training Logs, and other Investigator Site File (ISF) documents

Education

• Walden University

  Master’s Degree, Masters of Health Administration

• University of Wisconsin-Madison

  Bachelor’s Degree, Life Science/Biology

• Emory University

  Certificate, Business Intelligence