SMA I

As a SMA I you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities include receiving all study documentation from the Project Team, Client, or Clinical Research Associate, logging information into an internal tracking system, scanning documentation to the correct location in an electronic repository, setting up the Trial Master File (TMF) per the client-approved specifications and PRA standards, maintaining files, running monthly reports, delivering the Trial Master File at study closeout, and resolving internal quality control findings and audit findings. The role also involves running projections, creation of checklists, attending project calls with clinical team members, and the management of larger and/or more complex studies.