Archives: Speakers

A certified clinical research professional with more than 20 years of direct experience in clinical research within a large Academic Medical Center, private practice and hospital environments. Aryn’s experience includes: clinical research operations and administration, research compliance and oversight, protocol development, IRB submission and all regulatory maintenance, research coordination, grant writing and submissions, budget development, supervision and training of other research coordinators, site perspective of TMF and proficient knowledge of research regulations in FDA/GCP/ICH guidelines. Aryn possess excellent project, regulatory management and coordination skills; effective management proficiency of multi-protocol research from development to finalization. Aryn have great enthusiasm for my chosen field, pride in work standards, and the ability to translate enthusiasm into concrete, positive results.

Dr Clemens Busse is currently working as a Senior Client Manager, Medical Devices at BSI, covering EMEA. He has worked in the IVD industry since 2009 in responsible functions for design and development and quality control. His tasks involved research activities, project planning and budgeting, development planning, data evaluation, raw material validation, performance and stability studies, and product troubleshooting. The product range he was responsible for during his career covers manual assays to fully automated solutions. He obtained an engineering degree in Biotechnology, followed by a PHD from the German Cancer Research Center in Heidelberg, Germany, in molecular virology.

Insiya has a PhD from the University of Cambridge, England (Immunology NK cell research), Postdoctoral, Biotech and Clinical Research experience. Over 10 years of laboratory experience and strong research background and knowledge in the fields of virology, immunology (NK and T cell research) and oncology research with 8 peer reviewed published papers. Experience in coordinating clinical trials and overseen the startup and continuation of 15 clinical trial protocols simultaneously in a Phase I Cancer Program. Strong communication skills and the ability to explain complex technical information in simple language in order to facilitate user understanding and learning.