Jobs at PSI CRO

Supports clinical study startup in Australia by maintaining tracking systems, facilitating site budgets and contracts, collecting regulatory documents, preparing submission dossiers, coordinating with project teams and sites, developing activation timelines and enrollment projections, reviewing translations, and supervising Trial Master File maintenance. This is an 18-month contract based in Sydney with a hybrid work arrangement.

Supports clinical research projects by maintaining databases and tracking systems, managing documents, coordinating investigative site communications, resolving site queries, facilitating training and system access, administering vendor and site payments, and assisting with meetings and correspondence. The role requires strong organization, attention to detail, multitasking, interpersonal communication, and prior administrative experience in a clinical research or CRO environment.