Summary
Overview
Work History
Education
Skills
Affiliations
Timeline
Generic

Olumide Balogun

Summary

Highly skilled Clinical Database Manager with 8 years of experience overseeing large-scale databases in the clinical research sector. Expert in electronic data capture tools, including Oracle, RAVE, RDC, and Inform, with a proven track record in managing external vendors to ensure timely and accurate deliverables.

Strong and advanced technical proficiency in SQL, Python, and Power BI, combined with a solid understanding of database design, data modeling, and qualitative analysis. Adept at troubleshooting data access issues and maintaining data integrity, with a demonstrated ability to adapt to rapidly changing priorities and deadlines.

Overview

8
8
years of professional experience

Work History

Database Manager/Data Curation Specialist

TargetRWE
04.2021 - Current
  • Partner with business stakeholders to determine data needs and oversee overall data management
  • Ensured documentation and consistent maintenance of code, logs, and output within a regulated computing environment
  • Responsible for the study-specific data management tasks from protocol review to database lock to ensure data are collected, reviewed, and delivered with high quality, on-time, and within scope
  • Responsible for the accurate development of CRFs and edit specification per protocol and the completeness of user acceptance testing of CRFs and associated edit specifications for assigned clinical trials
  • Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer documents including import/export agreements and data specifications
  • Provide ad-hoc report development, and support database lock and archiving activities
  • Review and contributed as a member of the CRF development team to develop the data collection modules on assigned studies where protocol requirements are outside of standard CRF library versions
  • Ensure that medical coding is completed in a timely fashion, completed for all data cuts, and reviewed and approved by medical monitors
  • Ensure accuracy and completeness of data entry in EDC system using source data verification methods from medical records

Lead Clinical Data Manager

Covance
04.2018 - 04.2021
  • Led various aspects of study design, database setup, and database lock using EDC systems (Oracle, RDC, Inform, Rave).
  • Developed, reviewed, and maintained Study Specific Procedures.
  • Collaborated with Database Administrators to design clinical study databases in compliance with relevant protocols.
  • Reviewed SAS Proc contents, compared Data Listings with Test CRFs, and created safety signal detection snapshots for reviews.
  • Ensured CRF data completeness and accuracy; ran batch validations, generated manual queries, and resolved data discrepancies.
  • Updated and corrected data based on resolved queries, performing QC audits to establish accuracy rates.
  • Engaged with project teams, investigative site personnel, and third-party vendors to ensure alignment.
  • Trained Clinical Research Associates (CRAs) on data collection best practices, focusing on effective resolution of system-generated queries.
  • Managed the transition to electronic data capture systems, resulting in increased productivity and reduced manual errors.
  • Liaised with external vendors for seamless integration of third-party applications into existing workflows.

Clinical Data Associate-Remote

GRMS Pharma
07.2016 - 04.2018
  • Generated listings for manual data review
  • Completed necessary CRF tracking and update study metric
  • Generated data listings for External Data Reconciliation
  • Performed QC audits of the clinical trial database against the CRF and resolved queries to establish an accuracy rate
  • Performed additional data management activities as required
  • Updated, corrected, and reviewed data in the clinical database based on resolved data queries
  • Reviewed and compared Data Listing versus Test CRFs
  • Ran batch validations and generated manual queries according to procedure
  • Developed, reviewed, and maintained relevant Study Specific Procedures
  • Assisted the Database Administrator with the design of the clinical study database in accordance with relevant procedures
  • Conducted and documented User Acceptance Testing (UAT) and creation of UAT test script
  • Identified and resolved data discrepancies and apply Level 1 correction to CRFs as appropriate
  • Assisted in validation of edit checks
  • Accurately performed external data reconciliation in accordance with all applicable procedures
  • Assisted with development, review, and the update of relevant Data Management Study Specific Procedures

Education

Master of Science - Data Analytics

Northern Illinois University
Illinois

Bachelor of Science - Health Information Management (RHIA)

Chicago State University
Illinois

Skills

  • Data Visualization
  • Data Integration
  • Database Development and Administration
  • Agile Methodology
  • Tableau
  • Power BI
  • Data Quality Assurance and Security
  • SQL Proficiency
  • Metadata Management and
  • Data Governance
  • Python Programming
  • Data Modeling and Data Warehousing
  • SAS

Affiliations

  • American health Information Management Association(AHIMA)

Timeline

Database Manager/Data Curation Specialist

TargetRWE
04.2021 - Current

Lead Clinical Data Manager

Covance
04.2018 - 04.2021

Clinical Data Associate-Remote

GRMS Pharma
07.2016 - 04.2018

Master of Science - Data Analytics

Northern Illinois University

Bachelor of Science - Health Information Management (RHIA)

Chicago State University
Olumide Balogun