Bukkie Ojoawo is responsible for the coordination of all phases of clinical trials from start-up to closure. Manages, monitors, and reports research trial data to maintain quality and compliance. Assists in the development and design of research data collection tools, working with clinic staff to ensure ease of research project implementation, and project start up. Identified problems and/ or inconsistencies and monitor patients’ progress to include documentation and reporting of adverse events. Provides education/training for others within the department. Evaluates and analyzes clinical trial data to ensure accuracy and consistency between source documents as well as proper, timely reporting of critical study events. Develops and executes plans to ensure that all aspects of each study were completed with strict adherence to protocol.
Member, Society for Clinical Trials (SCT)
Member, American Society for Clinical Oncology (ASCO)
Member, Regulatory Affairs Regulatory Society (RARS)
Certified Associate in Project Management (CAPM)
Master of Health Sciences in Clinical Research Administration, Walden University
Postgraduate Certificate in Global Clinical Research, Harvard Medical School
Bachelor of Science in Chemistry/Biochemistry, Ladoke Akintola University of Technology, Nigeria