Ashley Thompson, MHA, CCRP joins CFRI as the new IRB regulatory coordinator. Ashley has more than 10 years of clinical research experience with a focus on leukemia, lymphoma, diagnostic imaging, epidemiology and public health. Prior to joining the CFRI, she gained extensive knowledge in clinical trial coordination, regulatory compliance and quantitative data analysis at St. Jude Children’s Research Hospital.
Celine Wu, MSc, joins CFRI as a clinical research coordinator. Celine gained experience in clinical trial management, including patient enrollment, event reporting and compliance from her previous role as a clinical research practitioner at the National Institute for Health Research Centers in London, England. Celine also has clinical and basic research experience in the field of immunology.
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