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

The Senior Clinical Research Associate will conduct site visits, ensure trial compliance, review data, and prepare study documentation.

The Senior Clinical Research Associate oversees and monitors clinical trials, ensures compliance with regulations, coordinates site activities, and manages trial-related issues effectively.

The Clinical Site Associate supports clinical trial operations, manages site communications, maintains documentation, and ensures compliance for site readiness.

The Clinical Research Associate will manage clinical trial processes including site visits, data integrity, and prepare study documentation to ensure compliance and patient safety.

The Clinical Research Associate will manage clinical trials, ensure compliance and data integrity, and collaborate with site staff and investigators.

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

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

As a Clinical Research Associate, you will be the primary contact between investigational sites and sponsors, ensure compliance, monitor safety, and assist with various site-related activities.

The Senior Biostatistician I will lead early phase clinical trials, provide statistical inputs for protocols and reports, and mentor junior statisticians.