Arman Abedin

Background

About Arman Abedin

Highly motivated and experienced (8+ years) Clinical Research Personnel with a demonstrated history of working in a patient centered clinical setting as well as within a multi-disciplinary research team in various settings (CRO, hospital, pharmaceutical). Knowledgeable of Clinical Research Methodology, Biotechnology and Pharmaceuticals with advanced knowledge of ICH-GCP and U.S. Food and Drug Administration (FDA) regulations. Highly adaptable, engaging, energized constantly looking for challenges and learning opportunities-Strong knowledge of ICH-GCP and Canadian/US regulatory requirements -Experience working within multidisciplinary teams, interdepartmentally and remotely following the VACC principles in various stages of a clinical trial -Demonstrated ability and experience in proving guidance to different stakeholders in conducting clinical research according to the federal and local regulations -Accumulated rich experience in essential clinical trial documentation including adverse event reporting, letters of agreement/contracts, as well as documents pertaining to REB approval -Experience in designing and developing study consent documents as well as study case report forms -SOCRA certified -Ability to generate accurate and timely reports based on protocol requirements -Experience collecting clinical samples, collecting data and data entry, data verification