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Lead contracting activities for global clinical studies, negotiate agreements, manage site budgets, and collaborate with key stakeholders to ensure alignment and efficiency in the contracting process.

The Regulatory Affairs Consultant will manage global labeling updates, ensure compliance with regulatory processes, and provide consulting services, leveraging 8+ years of experience to support product labeling initiatives and client needs.

The Senior Regulatory Affairs Associate coordinates regulatory submissions, maintains compliance, manages projects, and supports client relationships in regulatory matters.

The Clinical Operations Assistant supports clinical trial tasks by managing project documentation, coordinating site operations, assisting with training, and ensuring compliance with guidelines.

The Clinical Research Associate monitors clinical trials, maintains site integrity, ensures compliance, and resolves site issues while supporting investigators.

Oversee clinical trial monitoring activities, ensure compliance with regulations, manage investigator sites, and support recruitment initiatives while maintaining high operational standards.

The Senior Clinical Research Associate oversees clinical trial monitoring and site management, ensuring compliance with regulatory standards and facilitating communication among study teams and investigator sites.

As a Senior Regulatory Affairs Associate, develop CMC strategies, author regulatory submissions, manage change assessments, and lead project teams.