I am a dedicated clinical researcher with a strong record of designing, managing, and overseeing clinical studies across Phases I–IV. Holding dual ACRP certifications (ACRP-CP® and ACRP-PM®), I bring deep expertise in clinical trial operations, bioequivalence research, and regulatory compliance. As a Clinical and Projects Manager, I have led cross-functional teams, successfully executed complex clinical trials, and strengthened stakeholder engagement. I am highly skilled in project oversight, data analysis, and conflict management, consistently ensuring alignment with GCP, and international regulatory standards.
My commitment to ethical research and participant rights is reflected in my service on the Institutional Review Board (IRB) at the King Hussein Cancer Center, where I contributed to upholding rigorous ethical and regulatory guidelines for nearly three years.