Admin assistant for clinical trials - Exclusive for People With Disabilities

Update and maintain clinical documents and systems, such as the Trial Master File, to track site compliance and performance within project timelines. Prepare, handle, distribute, file, and archive clinical documentation and reports according to standard operating procedures. Assist Clinical Research Associates and Regulatory and Start-Up teams with tracking Case Report Forms, queries, and clinical data flow, while managing clinical trial supplies and maintaining tracking information. Serve as the central contact for designated project communications, correspondence, and associated documentation. Submit your CV and medical certification (laudo) when applying. This role is part of IQVIA's talent pool exclusively for people with disabilities.