Mariama Ibrahim
Clinical Research Associate ll @Duke Clinical Research Institute
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WORK HISTORY
Clinical Research Associate ll @Duke Clinical Research Institute
Conduct site selection, initiation and close-out monitoring visits, assess site compliance with the protocol, GCP, perform source document verification including inclusion/exclusion and SAEs, regulatory document review, drug accountability, recruitment and retention planning, and document appropriately. • Conduct in-house monitoring and site management activities, including review of eCRFs, resolution of follow-up items, subject visit compliance, and regulatory documents. • Effectively manage sites by identifying root causes for any problems, strategizing solutions, establishing and communicating a plan for improvement, collaborating with the PI to oversee progress, and following to resolution. • Coordinate the development and revision of protocols, ICFs, documentation and department standard operating procedures for the administration and monitoring the clinical trials.
EDUCATION
Wake Forest University Graduate School
Master's degree
The STEM Early College At North Carolina A&T State University
High School
North Carolina Agricultural and Technical State University
Bachelor’s Degree
East Carolina University
Cell/Cellular and Molecular Biology
ABOUT MARIAMA IBRAHIM
I am a graduate of East Carolina University where I received my undergraduate degree in Molecular Cell Biology and a Minor in Leadership Studies. I have also attended Wake Forest University where I received a Masters\'s Degree in Addiction Research and Clinical Health. Both of these degrees have afforded me the opportunity to acquire a diverse academic background in areas from microbiology to clinical health and be able to serve as a bridge between these two areas. My deepest desire is to utilize the knowledge and skillsets I have gained to benefit underserved minority populations as a practicing physician.
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