Description
Allucent is hiring a Senior Clinical Research Associate (SrCRA) for a hybrid role monitoring clinical trial sites on the east coast of Australia. The position independently oversees site initiation, routine monitoring, and close-out across study phases; ensures compliance with protocols, ICH-GCP, SOPs, and regulatory requirements; manages investigator relationships and data quality; resolves site issues; and supports regulatory affairs, site activation, contracting, and study start-up. At least seven years of onsite monitoring experience in Australia, strong ICH-GCP and regulatory knowledge, English communication skills, independent prioritization, and travel readiness are required.
