Sironax is seeking a proactive Clinical Research Associate (CRA) to join our team in Australia, overseeing in office monitoring of trial sites and ensuring compliance with ICH-GCP and Australian regulations. You will coordinate monitoring visits, SDV, IP accountability, TMF updates, and training site staff, working closely with investigators to support patient safety and data integrity.
The role requires 2–4 years of on-site CRA experience in a Sponsor or CRO, strong communication and analytical