Jobs at PSI CRO

Supports clinical trial startup in Australia by coordinating site contracts, budgets, regulatory submissions, documentation, timelines, enrollment projections, site activation milestones, translations, and Trial Master File maintenance. The role collaborates with project teams and investigational sites throughout the study lifecycle and requires clinical startup and ethics committee submission experience.

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