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.