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As a Clinical Research Associate, you will monitor clinical trials, ensuring adherence to protocols and regulations, conduct site visits, and train staff.

As a Global Study Manager, you will lead project execution, manage cross-functional teams, and develop strategies to meet project goals in the healthcare sector.

As a Global Study Manager, you will lead projects, manage cross-functional teams, and ensure successful project execution while mentoring team members.

The Clinical Research Associate will conduct and oversee clinical trials, ensuring compliance and data integrity while collaborating with site staff and investigators.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with sites; review data and support study documentation.

As a Clinical Research Associate, you will manage site interactions, ensure compliance with regulations, track training and budgets, and monitor patient safety throughout oncology trials.

As a Clinical Research Associate, you will monitor clinical trials, ensure compliance, collaborate with site staff, and manage data integrity.

The Senior CRA will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing multiple sites and projects.

As a Clinical Technology Specialist, you will lead the design and implementation of clinical systems, managing operations and ensuring compliance with regulations.

As a Global Study Manager at ICON, you will lead project management activities, develop plans, manage cross-functional teams, and ensure successful project execution.