Meyagabo Youbi

I’m a Clinical Research Associate (CRA) working across oncology and rare disease trials, focused on ensuring adherence to study protocols, regulatory requirements, and GCP. In my roles, I conduct site visits from recruitment through end of study to protect and safeguard the rights and well-being of human subjects.

At Syneoshealth (CRA 2) and ICON (CRA 2), I ensure the quality and integrity of reported data through site document review and site document verification, while also supporting site efficacy and drug accountability. I build continuous rapport with site teams to resolve study challenges efficiently and train/guide site staff to maintain high standards of clinical trial conduct using clinical trial guidelines and principles.

Previously at IQVIA (CRA 1), I performed site initiation, monitoring, and close-out visits, generated visit/contact reports, and supported enrollment timelines by developing patient strategies while staying compliant with approved SOPs, protocol, and GCP regulatory requirements. I’ve worked as lead monitor on multiple phase 2/3 studies (including prostate cancer, non-small lung cancer, breast cancer, hemophilia, head and neck cancer, fibrodysplasia ossificans progressiva, and lupus nephritis) and strengthen execution with CTMS/EDC and systems such as Veeva, Rave, Medidata, multiple IRT portals, TMF/eTMF platforms, Clario, and Advarra.