Majekodunmi Eguolo
@majekodunmieguolo
Experienced Clinical Research and Drug Safety professional.
United StatesWhat I'm looking for
I am an experienced Clinical Research and Drug Safety professional with a strong background in pharmacovigilance, adverse event reporting, and safety data analysis. My expertise includes managing electronic Trial Master Files (eTMF) and ensuring compliance with global regulatory requirements. I have hands-on experience using clinical data platforms and safety databases to track, assess, and report adverse drug reactions.
Throughout my career, I have demonstrated a keen attention to detail and leadership in quality control processes. I actively engage in advancing drug safety through professional memberships, research contributions, and peer-reviewed publications. My role at Colorado Prevention Center has allowed me to contribute significantly to global pharmacovigilance activities, ensuring compliance with international regulatory standards while leading efforts to improve safety processes.
Experience
Work history, roles, and key accomplishments
Clinical Research Drug Safety Associate
Colorado Prevention Center
Nov 2022 - Present (2 years 7 months)
Responsible for ensuring drug safety through processing safety reports, analyzing data, and maintaining regulatory compliance. Managed adverse event reports and contributed to quality control reviews of safety data. Led efforts to improve safety processes and provided training on pharmacovigilance procedures.
Capstone Project - eTMF Quality Control
Arizona State University, NuvOx Pharma
Jan 2025 - Feb 2025 (1 month)
Conducted quality control reviews of electronic Trial Master File documentation across clinical trial sites. Delivered regulatory gap analysis and proposed process improvements for audit readiness.
Quality Assurance and Control Associate
Medifast Inc
Jul 2018 - Jun 2021 (2 years 11 months)
Ensured compliance with GMP and regulatory standards in packaging operations. Conducted inspections on products, documented defects, and collaborated with teams for corrective actions. Trained staff in quality documentation practices and participated in continuous improvement initiatives.
Education
Degrees, certifications, and relevant coursework
AUArizona State University
Master of Science, Clinical Research Management
2023 - 2025
Grade: 4.0
Pursuing a Master of Science in Clinical Research Management & Regulatory Science with a focus on pharmacovigilance, adverse event reporting, and safety data analysis. Achieved a GPA of 4.0 while developing skills in managing electronic Trial Master Files and ensuring compliance with global regulatory requirements.
Tech stack
Software and tools used professionally
Availability
Location
United StatesAuthorized to work in
Job categories
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