Clinical Trial Assistant

Clinical Trial Assistant (IVD)Background: The client is a large medical device diagnostic company that works on a number of different therapeutic areas. They are in need of a specialized CTA to support their project.Project: This CTA will be responsible for coordination activities throughout the duration of the study. They will be responsible for activities including being part of the ETMF auditing system, Filing Trial Master Files (TMFs), reconfiguring TMFs, ensuring consistency and accuracy when maintaining file structure and handling sample collection/handling. The scope will also likely expand into responsibilities including site engagement and entry of medical data into the client’s EDC. This person will will also be responsible for handling shipping and receiving of on site deliveries. This consultant will need to have previous experience as a CTA for a medical device diagnostic company. This person will need to be on site 5 days a week at their Chaska MN site. Experience with an IVD Sponsor, specifically handling ETMF filing is a plus.Required:Diagnostics ExperienceSpecimen Collection/HandingLaboratory ExperienceBachelors Degree in scientific field