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The CRA II conducts site visits for qualification, initiation, monitoring, and closure, ensuring compliance with regulations and protocols, and managing site communications and activities throughout the study lifecycle.

Perform site qualification, monitoring, and management, ensuring compliance with regulatory requirements and protocol. Maintain accurate documentation and support project objectives through effective communication and site liaison.

The role involves managing site activities, ensuring compliance with protocols, maintaining project files, and supporting clinical monitoring staff. Minimal travel may be required.

The CRA II/ SCRA will perform site management, monitor compliance with regulations, manage clinical data, and communicate with study sites and project teams.

Perform site qualification, monitoring, and management activities for clinical trials, ensuring compliance with regulations and accuracy of data.

Lead interdisciplinary clinical research projects ensuring GCP/ICH compliance, deliverables, timelines, budgets, risk mitigation, TMF quality, client communications, business development support, and team leadership/mentoring.

The CRA II/ SCRA conducts site management activities, monitoring compliance with protocols and regulations, ensuring data integrity, and supporting clinical studies from initiation to close-out.

Conduct site monitoring activities including qualifications, initiation, and compliance checks, ensuring adherence to protocols and regulatory standards.