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The Senior CRA ensures quality execution at clinical trial sites, conducts oversight visits, supports compliance, and enhances quality performance across studies.

As a Clinical Site Associate, you will support clinical trial operations including site compliance, documentation management, and collaboration with Clinical Research Associates.

The Senior Clinical Research Associate will oversee clinical trial activities, ensuring adherence to protocols, conduct site visits, and manage data integrity while providing support and training to site staff.

Lead Clinical Research Associate will oversee and manage clinical trial sites, ensuring adherence to protocols and regulations while mentoring junior staff and ensuring data integrity.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and protocols while mentoring CRAs and collaborating with teams to execute trials effectively.

The Senior Clinical Research Associate will oversee clinical trials, ensuring compliance, maintaining data integrity, and preparing study documentation while collaborating with investigators and site staff.

Lead biostatistical components in clinical trials, oversee statistical activities, mentor junior statisticians, and ensure regulatory compliance.