Khaled al
Research Study Coordinator @Henry Ford Health
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WORK HISTORY
Research Study Coordinator @Henry Ford Health
US
Coordinate and oversee regulatory processes across multiple studies. • Prepare and submits regulatory documents to sponsors and IRB.• Work with clinical research team to ensure submission documents are up do date.• Obtain required signatures on regulatory documents and/or collaborates with Clinical Research Coordinators to secure them in a timely manner.• Maintain master files of all regulatory-related essential documents in both paper and electronic format.• Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.• Respond to queries in a timely manner.• Participate in monitoring visits and participate in multidisciplinary team program meetings as required.
EDUCATION
American Global Univerosty School of Medicine
Doctor Of Medicine
ABOUT KHALED AL
I bring a comprehensive understanding of both basic and clinical research as I have an excess of more than 10 years of experience within the healthcare industry, some of which being directly involved in clinical research. Successfully coordinating and managing up to 30 clinical research studies at a time throughout their full life cycle from subject recruitment to study completion, in Cardiology and Hematology/Oncology. Demonstrating an aptitude for overseeing daily clinical trial activities, including study start up, participant recruitment, reporting, meeting management, and policy implementation.
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