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The Site Partner II coordinates activities for timely site activation in clinical trials, serving as the main liaison for site issues, ensuring compliance with regulatory standards and maintaining documentation accuracy.

The Senior CRA monitors clinical trial sites, ensures compliance with protocols, trains site staff, and manages site relationships effectively.

As a Clinical Research Associate, you'll conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with investigators.

The Study Start-Up Lead will manage country-level study start-up activities, handle IRB submissions, ensure timely site selection, and improve operational processes.

The Senior Clinical Research Associate will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing relationships with sites and stakeholders.

As a Clinical Research Associate, you'll manage site operations for oncology trials, ensuring data quality and compliance, while collaborating with study teams.

As a Senior Contract Analyst, you will manage agreements, ensure compliance, and support project teams in contract interpretation and execution.